Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa

Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa

Retinitis pigmentosa (RP) is a leading cause of inherited blindness characterized by progressive degeneration of the retinal photoreceptor cells. This study aims to identify genetic mutations in a Chinese family RP-2236, an Indian family RP-IC-90 and 100 sporadic Indian individuals with autosomal re...

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Bibliographic Details
Main Authors: Yang, Yin, Yang, Yeming, Huang, Lulin, Zhai, Yaru, Li, Jie, Jiang, Zhilin, Gong, Bo, Fang, Hao, Kim, Ramasamy, Yang, Zhenglin, Sundaresan, Periasamy, Zhu, Xianjun, Zhou, Yu
Format: Online
Language:English
Published: Nature Publishing Group 2016
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037368/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037368/

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