共 50 条
- [32] A potential novel role of the R36P mutation in CRYGD in congenial cataract MOLECULAR VISION, 2024, 30 : 260 - 267
- [33] Novel missense mutation of major intrinsic protein gene in congenital cataract CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2020, 48 (07): : 996 - 998
- [36] A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family BMC MEDICAL GENETICS, 2018, 19
- [37] A missense mutation in the γD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q MOLECULAR VISION, 2004, 10 (21): : 155 - 162
- [38] A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family MOLECULAR VISION, 2012, 18 (50-51): : 465 - 470