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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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Detalhes bibliográficos
Main Authors: YI, JUNHUI, LI, SHIQIANG, JIA, XIAOYUN, XIAO, XUESHAN, WANG, PANFENG, GUO, XIANGMING, ZHANG, QINGJIONG
Formato: Artigo
Idioma:Inglês
Publicado em: D.A. Spandidos 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3573736/
https://ncbi.nlm.nih.gov/pubmed/22245991
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ijmm.2012.882
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