A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

We performed linkage analysis in a Belgian family with autosomal dominant midfrequency hearing loss, which has a prelingual onset and a nonprogressive course in most patients. We found LOD scores >6 with markers on chromosome 11q. Analysis of key recombinants maps this deafness gene (DFNA12) to a...

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Bibliografiska uppgifter
Huvudupphovsmän: Verhoeven, K, Van Camp, G, Govaerts, P J, Balemans, W, Schatteman, I, Verstreken, M, Van Laer, L, Smith, R J, Brown, M R, Van de Heyning, P H, Somers, T, Offeciers, F E, Willems, P J
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1997
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1712440/
https://ncbi.nlm.nih.gov/pubmed/9150164
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