A missense mutation in the γD-crystallin gene GRYGD associated with autosomal dominant congenital cataract in a Chinese family

Feng GuRong LiXi Xin MaLi Song ShiShang Zhi HuangXu Ma

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A missense mutation in the γD-crystallin gene GRYGD associated with autosomal dominant congenital cataract in a Chinese family

机译：中国家庭常染色体显性先天性白内障患者γD-晶状体蛋白基因GRYGD的错义突变

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《Molecular vision》 |2006年第2006期|共页
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Feng GuRong LiXi Xin MaLi Song ShiShang Zhi HuangXu Ma;
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中图分类生物化学;
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1. A missense mutation in the γD-crystallin gene GRYGD associated with autosomal dominant congenital cataract in a Chinese family [J] . Feng GuRong LiXi Xin MaLi Song ShiShang Zhi HuangXu Ma Molecular vision . 2006,第2006期

机译：中国家庭常染色体显性先天性白内障患者γD-晶状体蛋白基因GRYGD的错义突变
2. A missense mutation in the γD-crystallin gene GRYGDassociated with autosomal dominant congenital cataract in a Chinesefamily [J] . Molecular vision . 2006,第2006期

机译：中国家庭常染色体显性先天性白内障患者γD-晶状体蛋白基因GRYGD的错义突变
3. A missense mutation in the γD-crystallin gene GRYGDassociated with autosomal dominant congenital cataract in a Chinesefamily [J] . Molecular vision . 2006,第2006期

机译：中国家庭常染色体显性先天性白内障患者γD-晶状体蛋白基因GRYGD的错义突变
4. Functional consequences of missense mutation in the GJB2 gene associated with non-synclromic hearing loss [C] . Lee Kyu Yup, Choi Soo-Young, Lin Xi, Asia Pacific Symposium on Cochlear Implant and Related SciencesAsia Pacific Symposium on Cochlear Implant and Related Sciences . 2009

机译：与非辛瘤性听力损失相关的GJB2基因畸形突变的功能后果
5. Genomic study and mutation functional analysis of autosomal dominant congenital cataract. [D] . Zhang, Liyun. 2007

机译：常染色体显性先天性白内障的基因组研究和突变功能分析。
6. A novel mutation in γD-crystallin associated with autosomal dominant congenital cataract in a Chinese family [O] . Li Wang, Xueli Chen, Yi Lu, 2011

机译：中国家庭常染色体显性先天性白内障相关的γD-晶状蛋白新突变
7. Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract [O] . Ma, Z, Zheng, J, Yang, F, 2005

机译：中国常染色体显性遗传性先天性白内障家庭中连接蛋白基因的两个新突变

A missense mutation in the γD-crystallin gene GRYGD associated with autosomal dominant congenital cataract in a Chinese family

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