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A novel mutation in the RS1 gene in a Chinese family with X-linked congenital retinoschisis
The purpose of the present study was to assess the clinical characteristics of X-linked retinoschisis (XLRS) in a Chinese family over a 7-year period with the aim of identifying possible genetic mutations associated with this disease. A total of 2 male siblings from a family with XLRS were followed...
Uloženo v:
| Vydáno v: | Exp Ther Med |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
D.A. Spandidos
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7739845/ https://ncbi.nlm.nih.gov/pubmed/33335587 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2020.9556 |
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