Clinical findings and RS1 genotype in 90 Chinese families with X-linked retinoschisis

PURPOSE: X-linked retinoschisis (XLRS) is an early-onset retinal degenerative disorder caused by mutations in the RS1 gene. The objective of this study was to describe the clinical and genetic findings in 90 unrelated Chinese patients with XLRS. METHODS: All patients underwent clinical examination,...

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Detalles Bibliográficos
Autores principales: Chen, Chunjie, Xie, Yue, Sun, Tengyang, Tian, Lu, Xu, Ke, Zhang, Xiaohui, Li, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155891/
https://www.ncbi.nlm.nih.gov/pubmed/32300273

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155891/
https://www.ncbi.nlm.nih.gov/pubmed/32300273

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