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Clinical findings of end-stage retinitis pigmentosa with a homozygous PDE6A variant (p.R653X)
PURPOSE: To report clinical and genetic features of a Japanese patient with end-stage retinitis pigmentosa (RP) caused by a homozygous PDE6A variant. METHODS: We performed comprehensive ophthalmic examinations. Whole exome sequencing analysis was used to investigate the RP patient with parental cons...
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| Publicat a: | Am J Ophthalmol Case Rep |
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| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6307093/ https://ncbi.nlm.nih.gov/pubmed/30619975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajoc.2018.12.019 |
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