載入...

A novel mutation in the RS1 gene in a Chinese family with X-linked congenital retinoschisis

The purpose of the present study was to assess the clinical characteristics of X-linked retinoschisis (XLRS) in a Chinese family over a 7-year period with the aim of identifying possible genetic mutations associated with this disease. A total of 2 male siblings from a family with XLRS were followed...

全面介紹

Na minha lista:
書目詳細資料
發表在:Exp Ther Med
Main Authors: Zhang, Na, Peng, Yao, Zhou, Nan, Qi, Yanhua
格式: Artigo
語言:Inglês
出版: D.A. Spandidos 2021
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7739845/
https://ncbi.nlm.nih.gov/pubmed/33335587
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2020.9556
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!