Exome Sequencing Analysis Identifies Compound Heterozygous Mutation in ABCA4 in a Chinese Family with Stargardt Disease
文献类型：期刊论文
| 作者 | Zhou, Yu ; Tao, Siyu ; Chen, Hui ; Huang, Lulin ; Zhu, Xiong ; Li, Youping ; Wang, Zhili ; Lin, He ; Hao, Fang ; Yang, Zhenglin ; Wang, Liya ; Zhu, Xianjun |
| 刊名 | PLOS ONE
 |
| 出版日期 | 2014 |
| 卷号 | 9期号:3页码:e91962(1-8) |
| 产权排序 | 6 |
| 通讯作者 | Wang, LY (reprint author), Zhengzhou Univ, Peoples Hosp, Henan Eye Hosp, Zhengzhou, Henan, Peoples R China. |
| 合作状况 | 其它 |
| 英文摘要 | Stargardt disease is the most common cause of juvenile macular dystrophy. Five subjects from a two-generation Chinese family with Stargardt disease are reported in this study. All family members underwent complete ophthalmologic examinations. Patients of the family initiated the disease during childhood, developing progressively impaired central vision and bilateral atrophic macular lesions in the retinal pigmental epithelium (RPE) that resembled a "beaten-bronze'' appearance. Peripheral venous blood was obtained from all patients and their family members for genetic analysis. Exome sequencing was used to analyze the exome of two patients II1, II2. A total of 50709 variations shared by the two patients were subjected to several filtering steps against existing variation databases. Identified variations were verified in all family members by PCR and Sanger sequencing. Compound heterozygous variants p.Y808X and p.G607R of the ATP-binding cassette, sub-family A (ABC1), member 4 (ABCA4) gene, which encodes the ABCA4 protein, a member of the ATP-binding cassette (ABC) transport superfamily, were identified as causative mutations for Stargardt disease of this family. Our findings provide one novel ABCA4 mutation in Chinese patients with Stargardt disease. |
| 学科主题 | Multidisciplinary Sciences |
| 收录类别 | SCI |
| 语种 | 英语 |
| 公开日期 | 2016-02-26 |
| 源URL | [http://210.75.237.14/handle/351003/26692]  |
| 专题 | 成都生物研究所_天然产物研究 |
| 推荐引用方式 GB/T 7714 | Zhou, Yu,Tao, Siyu,Chen, Hui,et al. Exome Sequencing Analysis Identifies Compound Heterozygous Mutation in ABCA4 in a Chinese Family with Stargardt Disease[J]. PLOS ONE,2014,9(3):e91962(1-8). |
| APA | Zhou, Yu.,Tao, Siyu.,Chen, Hui.,Huang, Lulin.,Zhu, Xiong.,...&Zhu, Xianjun.(2014).Exome Sequencing Analysis Identifies Compound Heterozygous Mutation in ABCA4 in a Chinese Family with Stargardt Disease.PLOS ONE,9(3),e91962(1-8). |
| MLA | Zhou, Yu,et al."Exome Sequencing Analysis Identifies Compound Heterozygous Mutation in ABCA4 in a Chinese Family with Stargardt Disease".PLOS ONE 9.3(2014):e91962(1-8). |
入库方式： OAI收割
来源：成都生物研究所
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