Skip to main content
Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

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

Fig. 2

Pedigree and variants identified in crystallin genes These schematics show the encoded domain structure of CRYAA (a), CRYBA1 (b), CRYBA4 (c), CRYBB1 (d), CRYGC (e), and CRYGD (f). 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, −/− indicates individuals testing negative. WT: wild type, MT: mutant type

Back to article page

Orphanet Journal of Rare Diseases

ISSN: 1750-1172