Phenotype Heterogeneity and the Association Between Visual Acuity and Outer Retinal Structure in a Cohort of Chinese X-Linked Juvenile Retinoschisis Patients

Purpose: X-linked juvenile retinoschisis (XLRS), caused by mutations in the RS1 gene, is an X-linked recessive inherited disease that typically involves both eyes in the first 2 decades of life. Recently, the phenotype heterogeneity of this condition has drawn increasing attention. We reported vario...

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Detalles Bibliográficos
Autores principales: Guo, Qingge, Li, Ya, Li, Jiarui, You, Ya, Liu, Changgeng, Chen, Kang, Li, Shuyin, Lei, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931683/
https://www.ncbi.nlm.nih.gov/pubmed/35309139
http://dx.doi.org/10.3389/fgene.2022.832814

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931683/
https://www.ncbi.nlm.nih.gov/pubmed/35309139
http://dx.doi.org/10.3389/fgene.2022.832814

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