A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus

Non-syndromic hearing impairment is one of the most heterogeneous hereditary conditions, with more than 40 reported gene localisations. We have identified a large Dutch family with autosomal dominant non-syndromic sensorineural hearing impairment. In most patients, the onset of hearing impairment is...

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Autores principales: Van Camp, G., Kunst, H., Flothmann, K., McGuirt, W., Wauters, J., Marres, H., Verstreken, M., Bespalova, I., Burmeister, M., Van de Heyning, P. H, Smith, R., Willems, P., Cremers, C., Lesperance, M.
Formato: Artigo
Lenguaje:Inglês
Publicado: BMJ Group 1999
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Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734405/
https://ncbi.nlm.nih.gov/pubmed/10424813
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