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Fig. 5 | Orphanet Journal of Rare Diseases

Fig. 5

From: Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott–Aldrich syndrome

Fig. 5

a Mutations in WAS gene of the younger cousin (c.158 T > C in exon 2 and c.273 + 14C > T in intron 2); b Mutations in WAS gene of the cousin's mother (heterozygous mutation of c.158 T > C in exon 2 and c.273 + 14C > T in intron 2); c Mutations in WAS gene of the cousin’s sister (heterozygous mutation of c.158 T > C in exon 2 and c.273 + 14C > T in intron 2)

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172