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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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| Publicado no: | Mol Vis |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Molecular Vision
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7155891/ https://ncbi.nlm.nih.gov/pubmed/32300273 |
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