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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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Bibliografiska uppgifter
I publikationen:Sci Rep
Huvudupphovsmän: Hu, Qin-rui, Huang, Lv-zhen, Chen, Xiao-li, Xia, Hui-ka, Li, Tian-qi, Li, Xiao-xin
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group 2017
Ämnen:
Länkar: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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