Retinal Disease Course in Usher Syndrome 1B Due to MYO7A Mutations

PURPOSE. To determine the disease course in Usher syndrome type IB (USH1B) caused by myosin 7A (MYO7A) gene mutations. METHODS. USH1B patients (n = 33, ages 2–61) representing 25 different families were studied by ocular examination, kinetic and chromatic static perimetry, dark adaptometry, and opti...

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Detalhes bibliográficos
Main Authors: Jacobson, Samuel G., Cideciyan, Artur V., Gibbs, Dan, Sumaroka, Alexander, Roman, Alejandro J., Aleman, Tomas S., Schwartz, Sharon B., Olivares, Melani B., Russell, Robert C., Steinberg, Janet D., Kenna, Margaret A., Kimberling, William J., Rehm, Heidi L., Williams, David S.
Formato: Artigo
Idioma:Inglês
Publicado em: Association for Research in Vision and Ophthalmology, Inc. 2011
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3263772/
https://ncbi.nlm.nih.gov/pubmed/21873662
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.11-8313
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