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A Gene Scan Study of RPE65 in Chinese Patients with Leber Congenital Amaurosis
BACKGROUND: Leber congenital amaurosis (LCA) is a visual disease which is caused by RPE65 mutations and results in retinal degeneration and severe vision loss in early infancy. According to previous researches, mutations of the RPE65 gene account for 16% of all cases of LCA. This study aimed to iden...
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| Pubblicato in: | Chin Med J (Engl) |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Medknow Publications & Media Pvt Ltd
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5695057/ https://ncbi.nlm.nih.gov/pubmed/29133760 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0366-6999.218007 |
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