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PubMed for id: 334357
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Bioinformatics analysis of candidate genes and mutations in a congenital sensorineural hearing loss pedigree: detection of 52 genes for the DFNA52 locus.
J Laryngol Otol. 2008 Oct;122(10):1029-36. doi: 10.1017/S0022215107001582. Epub 2008 Feb 29.
J Laryngol Otol. 2008.
PMID: 18312703
[Mutation screening of 20 candidate genes located in chromo-some 5q31-5q32 for DFNA52 locus].
Bu FX, Peng Y, Wang SH, Pan Q, Hu ZM, Gong HY, Zhang J, Wu LQ, Liang DS, Pan Q, Feng Y, Xia K, Xia JH.
Bu FX, et al.
Yi Chuan. 2009 Jan;31(1):43-9. doi: 10.3724/sp.j.1005.2009.00043.
Yi Chuan. 2009.
PMID: 19138900
Chinese.
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A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
Xia J, Deng H, Feng Y, Zhang H, Pan Q, Dai H, Long Z, Tang B, Deng H, Chen Y, Zhang R, Zheng D, He Y, Xia K.
Xia J, et al.
J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098.
J Hum Genet. 2002.
PMID: 12522684
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