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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Main Authors: Heckenlively, J R, Chang, B, Erway, L C, Peng, C, Hawes, N L, Hageman, G S, Roderick, T H
Formáid: Artigo
Teanga:Inglês
Foilsithe: 1995
Ábhair:
Research Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC40579/
https://ncbi.nlm.nih.gov/pubmed/7479945
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