Citations for
1DFNA50, MIR96
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.
Soldà G, Robusto M, Primignani P, Castorina P, Benzoni E, Cesarani A, Ambrosetti U, Asselta R, Duga S.
Hum Mol Genet 21(3):577-85. doi: 10.1093/hmg/ddr493. Epub 2011 Oct 28. 2012
2DFNA50, MIR96
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.
Nat Genet at Genet. 2009 2009
3DFNA50
A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci.
Modamio-Hoybjor S, Moreno-Pelayo MA, Mencia A, del Castillo I, Chardenoux S, Morais D, Lathrop M, Petit C, Moreno F.
J Med Genet 41(2):e14. No abstract available. 2004