Molecular Diagnosis of Putative Stargardt Disease by Capture Next Generation Sequencing

Molecular Diagnosis of Putative Stargardt Disease by Capture Next Generation Sequencing

Stargardt Disease (STGD) is the commonest genetic form of juvenile or early adult onset macular degeneration, which is a genetically heterogeneous disease. Molecular diagnosis of STGD remains a challenge in a significant proportion of cases. To address this, seven patients from five putative STGD fa...

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Bibliographic Details
Main Authors: Zhang, Xiao, Ge, Xianglian, Shi, Wei, Huang, Ping, Min, Qingjie, Li, Minghan, Yu, Xinping, Wu, Yaming, Zhao, Guangyu, Tong, Yi, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Format: Online
Language:English
Published: Public Library of Science 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999032/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999032/

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