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Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa
PURPOSE: Retinitis pigmentosa (RP) is a genetically heterogeneous trait with autosomal-recessive (ar) inheritance underlying 50% of genetic disease cases. Sixty-one arRP genes have been identified, and recently, DHX38 has been reported as a potential candidate gene for arRP with only a single family...
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| Publicado no: | Invest Ophthalmol Vis Sci |
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| Main Authors: | , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Association for Research in Vision and Ophthalmology
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6133250/ https://ncbi.nlm.nih.gov/pubmed/30208423 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.18-23849 |
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