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Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber's congenital amaurosis in unrelated Chinese patients
Huang, Hui[1]; Wang, Ying[2,3]; Chen, Huishuang[1]; Chen, Yanhua[1,4]; Wu, Jing[1]; Chiang, Pei-Wen[5]; Fan, Ning[2]; Su, Yan[1]; Deng, Jianlian[1]; Chen, Dongna[1]
2017
卷号8期号:21页码:35176
URL标识查看原文
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/4299527
专题暨南大学
作者单位1.[1]BGI Shenzhen, Shenzhen, Peoples R China
2.[2]Jinan Univ, Shenzhen Eye Hosp, Shenzhen Key Lab Ophthalmol, Shenzhen, Peoples R China
3.[3]Shenzhen Univ, Coll Optoelect Engn, Minist Educ & Guangdong Prov, Key Lab Optoelect Devices & Syst, Shenzhen, Peoples R China
4.[4]South China Univ Technol, Sch Biosci & Bioengn, Guangzhou, Guangdong, Peoples R China
5.[5]Casey Eye Inst Mol Diagnost Lab, Portland, OR USA
6.[6]Univ Chinese Acad Sci, BGI Educ Ctr, Shenzhen, Peoples R China
7.[7]Hong Kong Polytech Univ, Dept Appl Biol Chem Technol, Kowloon, Hong Kong, Peoples R China
8.[8]Zhejiang Univ, Sch Basic Med Sci, Hangzhou, Zhejiang, Peoples R China
9.[9]Univ Rochester, Med Ctr, Dept Pathol & Lab Med, Funct Genom Ctr, West Henrietta, NY USA
10.[10]Shenzhen Univ, Sch Ophthalmol & Optometry, Shenzhen, Peoples R China
推荐引用方式
GB/T 7714
Huang, Hui[1],Wang, Ying[2,3],Chen, Huishuang[1],et al. Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber's congenital amaurosis in unrelated Chinese patients[J],2017,8(21):35176.
APA Huang, Hui[1].,Wang, Ying[2,3].,Chen, Huishuang[1].,Chen, Yanhua[1,4].,Wu, Jing[1].,...&Liu, Xuyang[2,10].(2017).Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber's congenital amaurosis in unrelated Chinese patients.,8(21),35176.
MLA Huang, Hui[1],et al."Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber's congenital amaurosis in unrelated Chinese patients".8.21(2017):35176.
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