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Figure 3 | Orphanet Journal of Rare Diseases

Figure 3

From: Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics

Figure 3

Pedigrees of Families 1 (A), 2 (B), 3 (C), 4 (D) and 5 (E). Affected individuals are indicated by filled symbols and index patients by an arrow. In the genotype M stands for the mutant allele (c.640_656dup in Families 1–4 and c.573del in Family 5) and + for the wild-type allele.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172