A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

The sixteenth gene to cause autosomal dominant nonsyndromic hearing loss (ADNSHL), DFNA16, maps to chromosome 2q23-24.3 and is tightly linked to markers in the D2S2380-D2S335 interval. DFNA16 is unique in that it results in the only form of ADNSHL in which the phenotype includes rapidly progressing...

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Main Authors: Fukushima, K, Kasai, N, Ueki, Y, Nishizaki, K, Sugata, K, Hirakawa, S, Masuda, A, Gunduz, M, Ninomiya, Y, Masuda, Y, Sato, M, McGuirt, W T, Coucke, P, Van Camp, G, Smith, R J
Formato: Artigo
Idioma:Inglês
Publicado: 1999
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378084/
https://ncbi.nlm.nih.gov/pubmed/10364526
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