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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Detalles Bibliográficos
Autores principales: Jin, Zi-Bing, Huang, Xiu-Feng, Lv, Ji-Neng, Xiang, Lue, Li, Dong-Qing, Chen, Jiangfei, Huang, Changjiang, Wu, Jinyu, Lu, Fan, Qu, Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974215/
https://www.ncbi.nlm.nih.gov/pubmed/24670872
http://dx.doi.org/10.1038/ncomms4517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974215/
https://www.ncbi.nlm.nih.gov/pubmed/24670872
http://dx.doi.org/10.1038/ncomms4517

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