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Mutations in the RS1 gene in a Chinese family with X-linked juvenile retinoschisis
The purpose of our study was to identify the mutations in the retinoschisis 1 (RS1) gene, which was associated with X-linked retinoschisis (XLRS) in a four-generation Chinese family, and to provide the theoretical basis for gene diagnosis and gene therapy. Genomic DNA was extracted from peripheral l...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4204588/ https://ncbi.nlm.nih.gov/pubmed/25343070 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2012.v1.1.30 |
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