Citations for
1DFNA41, P2RX2
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss.
Faletra F, Girotto G, D'Adamo AP, Vozzi D, Morgan A, Gasparini P.
Gene 534(2):236-9. doi: 10.1016/j.gene.2013.10.052. Epub 2013 Nov 6. 2014
2DFNA41, P2RX2
Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noise.
Yan D, Zhu Y, Walsh T, Xie D, Yuan H, Sirmaci A, Fujikawa T, Wong AC, Loh TL, Du L, Grati M, Vlajkovic SM, Blanton S, Ryan AF, Chen ZY, Thorne PR, Kachar B, Tekin M, Zhao HB, Housley GD, King MC, Liu XZ.
Proc Natl Acad Sci U S A 110(6):2228-33. doi: 10.1073/pnas.1222285110. Epub 2013 Jan 23. 2013
3DFNA41
Refinement of the DFNA41 locus and candidate genes analysis.
Yan D, Ouyang XM, Zhu X, Du LL, Chen ZY, Liu XZ.
J Hum Genet 50(10):516-22. Epub 2005 Sep 30. 2005
4DFNA41
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter.
Blanton SH, Liang CY, Cai MW, Pandya A, Du LL, Landa B, Mummalanni S, Li KS, Chen ZY, Qin XN, Liu YF, Balkany T, Nance WE, Liu XZ.
J Med Genet 39(8):567-70. 2002