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Gene panel sequencing in Brazilian patients with retinitis pigmentosa
BACKGROUND: Retinal dystrophies constitute a group of diseases characterized by clinical variability and pronounced genetic heterogeneity. Retinitis pigmentosa is the most common subtype of hereditary retinal dystrophy and is characterized by a progressive loss of peripheral field vision (Tunnel Vis...
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| Publicado no: | Int J Retina Vitreous |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5592712/ https://ncbi.nlm.nih.gov/pubmed/28912962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40942-017-0087-6 |
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