Congenital cataract (CC) is the leading cause of visual disability in children. To date, mutations in many genes have been linked to CC. In a four-generation Chinese family with congenital nuclear pulverulent and posterior polar cataracts, we detected a heterozygous c.5G>A transition in the second e
β¦ LIBER β¦
Novel OTX2 mutation associated with congenital anophthalmia and microphthalmia in a Han Chinese family
β Scribed by Tian You; Yuan Lv; Shuqun Liu; Fei Li; Yan Zhao; Jingyu Lv; Guangrong Qiu; Jesse Li-Ling
- Book ID
- 114925126
- Publisher
- Wiley (Blackwell Publishing)
- Year
- 2012
- Tongue
- English
- Weight
- 224 KB
- Volume
- 90
- Category
- Article
- ISSN
- 1755-375X
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