Four novel RS1 gene mutations in Polish patients with X-linked juvenile retinoschisis

PURPOSE: To determine the clinical features and to identify mutations in the retinoschisis gene (RS1) in ten patients with X-linked retinoschisis (XLRS). METHODS: Ten male patients from nine Polish families were included in this study. Ophthalmologic examinations, including optical coherence tomogra...

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Detalles Bibliográficos
Autores principales: Skorczyk, Anna, Krawczyński, Maciej R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534142/
https://www.ncbi.nlm.nih.gov/pubmed/23288992

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