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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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| Hauptverfasser: | , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
D.A. Spandidos
2012
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| Schlagworte: | |
| Online Zugang: | 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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