Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations

PURPOSE: Previously, patients with RHO mutations and a class A phenotype were found to have severe early-onset loss of rod function, whereas patients with a class B phenotype retained rod function at least in certain retinal regions. Here class B patients were studied at different disease stages to...

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Detaylı Bibliyografya
Yayımlandı:Invest Ophthalmol Vis Sci
Asıl Yazarlar: Jacobson, Samuel G., McGuigan, David B., Sumaroka, Alexander, Roman, Alejandro J., Gruzensky, Michaela L., Sheplock, Rebecca, Palma, Judy, Schwartz, Sharon B., Aleman, Tomas S., Cideciyan, Artur V.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Association for Research in Vision and Ophthalmology 2016
Konular:
Retina
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5032913/
https://ncbi.nlm.nih.gov/pubmed/27654411
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.16-19890
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