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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: 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.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: BMJ Group 1999
विषय:
Original Articles
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734405/
https://ncbi.nlm.nih.gov/pubmed/10424813
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