Evidence for a fourth locus in Usher syndrome type I.

Usher syndrome type I (US1) is an autosomal recessive condition in which three different genes have been already localised (USH1A, USH1B, and USH1C on chromosomes 14q32, 11q13, and 11p15 respectively). The genetic heterogeneity of US1 has been confirmed in a previous study by linkage analysis of 20...

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Detalhes bibliográficos
Main Authors: Gerber, S, Larget-Piet, D, Rozet, J M, Bonneau, D, Mathieu, M, Der Kaloustian, V, Munnich, A, Kaplan, J
Formato: Artigo
Idioma:Inglês
Publicado em: 1996
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051818/
https://ncbi.nlm.nih.gov/pubmed/8825055
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