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Fig. 4 | Orphanet Journal of Rare Diseases

Fig. 4

From: Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract

Fig. 4

Pedigree and variants in BFSP2, FYCO1, GCNT2, and MIP. These schematics show the encoded domain structure of BFSP2 (a), exonic and protein domain structure of FYCO1 (b), encoded protein domain structure of GCNT2 (c) and MIP (d). Mutations found in this study are illustrated above the schematics, with novel variants indicated in red characters. Probands are indicated by arrows, +/− indicates heterozygous individuals, −/− for individuals testing negative. WT: wild type, MT: mutant type, W1: Wild Type 1, W2: Wild Type 2, M1: Mutant Type 1, M2: Mutant Type 2

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172