Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

Usher syndrome is a group of diseases with autosomal recessive inheritance, congenital hearing loss, and the development of retinitis pigmentosa, a progressive retinal degeneration characterized by night blindness and visual field loss over several decades. The causes of Usher syndrome are unknown a...

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Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Heckenlively, J R, Chang, B, Erway, L C, Peng, C, Hawes, N L, Hageman, G S, Roderick, T H
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 1995
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC40579/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7479945/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.92.24.11100
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