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Genetic analysis and clinical features of X-linked retinoschisis in Chinese patients
Many mutations in the retinoschisis (RS1) gene have been identified, but there are limited clinical data relating to the different genotypes. This study investigated the genotype, clinical phenotype and therapies for X-linked juvenile retinoschisis (XLRS) patients in China to evaluate the effects of...
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| Publicat a: | Sci Rep |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5341047/ https://ncbi.nlm.nih.gov/pubmed/28272453 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep44060 |
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