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Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome

Genome Medicine volume 11, Article number: 16 (2019) Cite this article

The Original Article was published on 28 February 2019

Correction to: Genome Med (2019) 11:12

https://doi.org/10.1186/s13073-019-0623-0

It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated.

Correct statement:

“Of note, subject 17 of our cohort presented with mild delayed motor milestones, generalized hypotonia, and, in particular, dysmorphic features including midface hypoplasia, tented upper lips, along with sleep issues, ASD, food-seeking behavior, and aggressive behavior; these clinical features are similar to those reported in SMS.”

Reference

  1. Vetrini F, et al. De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome. Genome Med. 2019;11:12. https://doi.org/10.1186/s13073-019-0623-0.

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Authors and Affiliations

  1. Baylor Genetics, Houston, TX, 77021, USA

    Francesco Vetrini, Wenmiao Zhu, Sarah H. Elsea, Weimin Bi, Seema Lalani, Fan Xia, Yaping Yang, Christine M. Eng, James R. Lupski & Pengfei Liu

  2. Northern Ireland Regional Genetics Service, Belfast City Hospital, Belfast, UK

    Shane McKee & Vivienne McConnell

  3. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA

    Jill A. Rosenfeld, Andrea M. Lewis, Kimberly Margaret Nugent, Elizabeth Roeder, Rebecca O. Littlejohn, Joseph T. Alaimo, Brett Graham, Daryl A. Scott, Lindsay C. Burrage, Donna M. Muzny, Richard A. Gibbs, Sarah H. Elsea, Jennifer E. Posey, Weimin Bi, Seema Lalani, Fan Xia, Yaping Yang, Christine M. Eng, James R. Lupski & Pengfei Liu

  4. Nottingham Genetics Service, Nottingham City Hospital, Nottingham, UK

    Mohnish Suri

  5. Department of Pediatrics, Baylor College of Medicine, San Antonio, TX, 78207, USA

    Kimberly Margaret Nugent, Elizabeth Roeder & Rebecca O. Littlejohn

  6. North West Thames Regional Genetics Service, 759 Northwick Park Hospital, London, UK

    Sue Holder & Birgitta Bernhard

  7. Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA

    Donna M. Muzny, Richard A. Gibbs & James R. Lupski

  8. Dell Children’s Medical Group, Austin, TX, 78723, USA

    Jill M. Harris & James B. Gibson

  9. Division of Genetic and Genomic Medicine, Nationwide Children’s Hospital; and Department of Pediatrics, College of Medicine, Ohio State University, Columbus, OH, 43205, USA

    Matthew Pastore & Kim L. McBride

  10. Department of Pediatrics, College of Medicine & Health Sciences, United Arab University, Al Ain, UAE

    Makanko Komara & Lihadh Al-Gazali

  11. Department of Pediatrics, Tawam Hospital, Al-Ain, UAE

    Aisha Al Shamsi

  12. Department of Pediatrics, Section of Genetics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA

    Elizabeth A. Fanning & Klaas J. Wierenga

  13. Department of Human Genetics and Metabolic Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel

    Ziva Ben-Neriah & Vardiella Meiner

  14. Department of Pediatrics, Texas Children’s Hospital, Houston, TX, 77030, USA

    J. Lloyd Holder Jr, Seema Lalani & James R. Lupski

  15. Department of Pediatrics, University of Hawaii, Honolulu, HI, 96826, USA

    Laurie H. Seaver

  16. Centre de Génétique Humaine, Université de Franche-Comté, Besançon, France

    Lionel Van Maldergem

  17. Department of Neurology, Boston Children’s Hospital, Boston, MA, 0211, USA

    Sonal Mahida, Janet S. Soul & Margaret Marlatt

  18. Gene DX, Gaithersburg, MD, 20877, USA

    Ludmila Matyakhina

  19. West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Women’s and Children’s Hospitals NHS Foundation Trust, Birmingham, UK

    Julie Vogt

  20. East Anglia Regional Genetics Service, Addenbrooke’s Hospital, Cambridge, UK

    June-Anne Gold & Soo-Mi Park

  21. All-Wales Medical Genetics Service, University Hospital of Wales, Cardiff, UK

    Vinod Varghese

  22. South East of Scotland Clinical Genetic Service, Western General Hospital, Edinburgh, UK

    Anne K. Lampe

  23. North East Thames Regional Genetics Service, Great Ormond Street Hospital, London, UK

    Ajith Kumar & Melissa Lees

  24. South East Thames Regional Genetics Service, Guy’s Hospital, London, UK

    Muriel Holder-Espinasse

  25. Oxford Regional Genetics Service, Oxford University Hospitals, Oxford, UK

    Ed Blair

  26. Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK

    Victoria Harrison

  27. The Hebrew University of Jerusalem, Jerusalem, Israel

    Hanoch Cassuto

  28. Monique and Jacques Roboh Department of Genetic Research, Hadassah-Hebrew University Medical Center, 91120, Jerusalem, Israel

    Orly Elpeleg

  29. Present address: Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, 46202, USA

    Francesco Vetrini & Brett Graham

  30. Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, 77030, USA

    Daryl A. Scott

  31. Present address: Mayo Clinic Florida, Department of Clinical Genomics, Jacksonville, FL, 32224, USA

    Klaas J. Wierenga

Authors
  1. Francesco Vetrini
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  2. Shane McKee
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  3. Jill A. Rosenfeld
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  4. Mohnish Suri
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  5. Andrea M. Lewis
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  6. Kimberly Margaret Nugent
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  7. Elizabeth Roeder
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  8. Rebecca O. Littlejohn
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  9. Sue Holder
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  10. Wenmiao Zhu
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  11. Joseph T. Alaimo
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  12. Brett Graham
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  13. Jill M. Harris
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  14. James B. Gibson
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  15. Matthew Pastore
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  16. Kim L. McBride
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  17. Makanko Komara
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  18. Lihadh Al-Gazali
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  19. Aisha Al Shamsi
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  20. Elizabeth A. Fanning
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  21. Klaas J. Wierenga
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  22. Daryl A. Scott
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  23. Ziva Ben-Neriah
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  24. Vardiella Meiner
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  25. Hanoch Cassuto
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  26. Orly Elpeleg
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  27. J. Lloyd Holder Jr
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  28. Lindsay C. Burrage
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  29. Laurie H. Seaver
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  30. Lionel Van Maldergem
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  31. Sonal Mahida
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  32. Janet S. Soul
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  33. Margaret Marlatt
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  34. Ludmila Matyakhina
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  35. Julie Vogt
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  36. June-Anne Gold
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  37. Soo-Mi Park
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  38. Vinod Varghese
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  39. Anne K. Lampe
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  40. Ajith Kumar
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  41. Melissa Lees
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  42. Muriel Holder-Espinasse
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  43. Vivienne McConnell
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  44. Birgitta Bernhard
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  45. Ed Blair
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  46. Victoria Harrison
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  47. Donna M. Muzny
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  48. Richard A. Gibbs
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  49. Sarah H. Elsea
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  50. Jennifer E. Posey
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  51. Weimin Bi
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  52. Seema Lalani
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  53. Fan Xia
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  54. Yaping Yang
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  55. Christine M. Eng
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  56. James R. Lupski
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  57. Pengfei Liu
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Consortia

The DDD study

Corresponding author

Correspondence to Pengfei Liu.

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Vetrini, F., McKee, S., Rosenfeld, J.A. et al. Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome. Genome Med 11, 16 (2019). https://doi.org/10.1186/s13073-019-0630-1

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  • DOI: https://doi.org/10.1186/s13073-019-0630-1

Genome Medicine

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