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....

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Hauptverfasser: Sullivan, Lori S., Heckenlively, John R., Bowne, Sara J., Zuo, Jian, Hide, Winston A., Gal, Andreas, Denton, Michael, Inglehearn, Chris F., Blanton, Susan H., Daiger, Stephen P.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1999
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Article
Online Zugang: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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