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...

ver descrição completa

Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Heckenlively, J R, Chang, B, Erway, L C, Peng, C, Hawes, N L, Hageman, G S, Roderick, T H
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1995
Assuntos:	Research Article
Acesso em linha:	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
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!