DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary Hearing Impairment, Maps to 12q21-24

Using linkage analysis, we identified a novel dominant locus, DFNA25, for delayed-onset, progressive, high-frequency, nonsyndromic sensorineural hearing loss in a large, multigenerational United States family of Czech descent. On the basis of recombinations in affected individuals, we determined tha...

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Detalhes bibliográficos
Main Authors: Greene, Charles C., McMillan, Pamella M., Barker, Susan E., Kurnool, Purnima, Lomax, Margaret I., Burmeister, Margit, Lesperance, Marci M.
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2001
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1234922/
https://ncbi.nlm.nih.gov/pubmed/11115382
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