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2009 | 1 |
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A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci.
J Med Genet. 2004 Feb;41(2):e14. doi: 10.1136/jmg.2003.012500.
J Med Genet. 2004.
PMID: 14757864
Free PMC article.
No abstract available.
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.
Mencía A, Modamio-Høybjør S, Redshaw N, Morín M, Mayo-Merino F, Olavarrieta L, Aguirre LA, del Castillo I, Steel KP, Dalmay T, Moreno F, Moreno-Pelayo MA.
Mencía A, et al.
Nat Genet. 2009 May;41(5):609-13. doi: 10.1038/ng.355. Epub 2009 Apr 12.
Nat Genet. 2009.
PMID: 19363479
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