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Genetic analysis and clinical features of X-linked retinoschisis in Chinese patients

Many mutations in the retinoschisis (RS1) gene have been identified, but there are limited clinical data relating to the different genotypes. This study investigated the genotype, clinical phenotype and therapies for X-linked juvenile retinoschisis (XLRS) patients in China to evaluate the effects of...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Hu, Qin-rui, Huang, Lv-zhen, Chen, Xiao-li, Xia, Hui-ka, Li, Tian-qi, Li, Xiao-xin
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5341047/
https://ncbi.nlm.nih.gov/pubmed/28272453
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep44060
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