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Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa
Inherited retinal diseases are a common cause of visual impairment in children and young adults, often resulting in severe loss of vision in later life. The most frequent form of inherited retinopathy is retinitis pigmentosa (RP), with an approximate incidence of 1 in 3,500 individuals worldwide1,2....
Bewaard in:
| Hoofdauteurs: | , , , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
1999
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2582380/ https://ncbi.nlm.nih.gov/pubmed/10391212 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/10314 |
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