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Bioinformatic Analysis of GJB2 Gene Missense Mutations.
Cell Biochem Biophys. 2015 Apr;71(3):1623-42. doi: 10.1007/s12013-014-0385-7.
Cell Biochem Biophys. 2015.
PMID: 25388846
Particular distribution of the GJB2/GJB6 gene mutations in Mexican population with hearing impairment.
Loeza-Becerra F, Rivera-Vega Mdel R, Martínez-Saucedo M, Gonzalez-Huerta LM, Urueta-Cuellar H, Berrruecos-Villalobos P, Cuevas-Covarrubias S.
Loeza-Becerra F, et al.
Int J Pediatr Otorhinolaryngol. 2014 Jul;78(7):1057-60. doi: 10.1016/j.ijporl.2014.04.002. Epub 2014 Apr 12.
Int J Pediatr Otorhinolaryngol. 2014.
PMID: 24774219
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GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment.
Dai P, Yu F, Han B, Liu X, Wang G, Li Q, Yuan Y, Liu X, Huang D, Kang D, Zhang X, Yuan H, Yao K, Hao J, He J, He Y, Wang Y, Ye Q, Yu Y, Lin H, Liu L, Deng W, Zhu X, You Y, Cui J, Hou N, Xu X, Zhang J, Tang L, Song R, Lin Y, Sun S, Zhang R, Wu H, Ma Y, Zhu S, Wu BL, Han D, Wong LJ.
Dai P, et al.
J Transl Med. 2009 Apr 14;7:26. doi: 10.1186/1479-5876-7-26.
J Transl Med. 2009.
PMID: 19366456
Free PMC article.
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DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls.
Tang HY, Fang P, Ward PA, Schmitt E, Darilek S, Manolidis S, Oghalai JS, Roa BB, Alford RL.
Tang HY, et al.
Am J Med Genet A. 2006 Nov 15;140(22):2401-15. doi: 10.1002/ajmg.a.31525.
Am J Med Genet A. 2006.
PMID: 17041943
Free PMC article.
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