A new locus for nonsyndromic deafnessDFNB51 maps to chromosome 11p13-p12
- 12 September 2005
- journal article
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 138A (4), 392-395
- https://doi.org/10.1002/ajmg.a.30949
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereociliaNature, 2005
- Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directlyHuman Molecular Genetics, 2004
- Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessJournal of Medical Genetics, 2003
- The molecular architecture of the inner earBritish Medical Bulletin, 2002
- Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeHuman Genetics, 2001
- The HUGO Gene Nomenclature Committee (HGNC)Human Genetics, 2001
- Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafnessJournal of Medical Genetics, 2001
- Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessNature Genetics, 2001
- Regulation of cortical structure by the ezrin-radixin-moesin protein familyCurrent Opinion in Cell Biology, 1999
- Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3Science, 1998