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Fig. 3 | Genome Medicine

Fig. 3

From: B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycanopathies

Fig. 3

Complementation of B3GALNT2-deficient HAP1 cells. a–g IIH6 FACS analysis of HAP1 B3GALNT2-deficient cell lines (ΔB3GALNT2) (a) complemented with WT (b) and different B3GALNT2 mutants (c–g). Percentages of IIH6-positive (upper right corner) and IIH6-negative (upper left corner) are given. The fluorescent signal of WT cells incubated with only the secondary antibody was used to determine the percentage of IIH6-positive cells

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Genome Medicine

ISSN: 1756-994X

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