Citations for
1DFNA57, DFNB15
[A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15]
Bönsch D, Schmidt CM, Scheer P, Bohlender J, Neumann C, am Zehnhoff-Dinnesen A, Deufel T.
HNO 56(2):177-82. German. 2008
2DFNA8, DFNB15, DM2
A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.
Bonsch D, Scheer P, Neumann C, Lang-Roth R, Seifert E, Storch P, Weiller C, Lamprecht-Dinnesen A, Deufel T.
Eur J Hum Genet 9(3):165-70. 2001
3DFNB41, MYO1F, DFNB15
MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.
Chen AH, Stephan DA, Hasson T, Fukushima K, Nelissen CM, Chen AF, Jun AI, Ramesh A, Van Camp G, Smith RJ.
Arch Otolaryngol Head Neck Surg 127(8):921-5. 2001
4DFN2, DFNA10, DFNA13, DFNA18, DFNA2, DFNA4, DFNA5, DFNA6, DFNB12, DFNB13, DFNB15, DFNB16, DFNB17, DFNB19, DFNB6, DFNB7, DFNB8, USH1D, USH1E, USH1F, CLRN1
Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness.
Skvorak AB, et al.
Hum Mol Genet 8(3):439-52 1999
5DFNB41, DFNB15
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.
Chen A, Wayne S, Bell A, Ramesh A, Srisailapathy CR, Scott DA, Sheffield VC, Van Hauwe P, Zbar RI, Ashley J, Lovett M, Van Camp G, Smith RJ.
Am J Med Genet 71(4):467-71. 1997