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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Qin-rui, Huang, Lv-zhen, Chen, Xiao-li, Xia, Hui-ka, Li, Tian-qi, Li, Xiao-xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341047/
https://www.ncbi.nlm.nih.gov/pubmed/28272453
http://dx.doi.org/10.1038/srep44060

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341047/
https://www.ncbi.nlm.nih.gov/pubmed/28272453
http://dx.doi.org/10.1038/srep44060

Ejemplares similares