Novel RS1 mutations associated with X-linked juvenile retinoschisis

To identify mutations in the retinoschisin (RS1) gene in families with X-linked retinoschisis (XLRS). Twenty families with XLRS were enrolled in this study. All six coding exons and adjacent intronic regions of RS1 were amplified by polymerase chain reaction (PCR). The nucleotide sequences of the am...

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Detalles Bibliográficos
Autores principales: YI, JUNHUI, LI, SHIQIANG, JIA, XIAOYUN, XIAO, XUESHAN, WANG, PANFENG, GUO, XIANGMING, ZHANG, QINGJIONG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2012
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573736/
https://www.ncbi.nlm.nih.gov/pubmed/22245991
http://dx.doi.org/10.3892/ijmm.2012.882

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573736/
https://www.ncbi.nlm.nih.gov/pubmed/22245991
http://dx.doi.org/10.3892/ijmm.2012.882

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