SLC7A14 linked to autosomal recessive retinitis pigmentosa

SLC7A14 linked to autosomal recessive retinitis pigmentosa

Retinitis pigmentosa (RP) is characterized by degeneration of the retinal photoreceptors and is the leading cause of inherited blindness worldwide. Although few genes are known to cause autosomal recessive RP (arRP), a large proportion of disease-causing genes remain to be revealed. Here we report t...

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Bibliographic Details
Main Authors: Jin, Zi-Bing, Huang, Xiu-Feng, Lv, Ji-Neng, Xiang, Lue, Li, Dong-Qing, Chen, Jiangfei, Huang, Changjiang, Wu, Jinyu, Lu, Fan, Qu, Jia
Format: Online
Language:English
Published: Nature Pub. Group 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974215/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974215/

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