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非综合征型常染色体显性遗传性耳聋的研究进展

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出处 《中华耳科学杂志》 CSCD 2005年第2期150-156,共7页 Chinese Journal of Otology
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参考文献30

  • 1[1]Lynch ED, Lee MK, Morrow JE, et al. Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous. Science., 1997 Nov 14; 278:1315-1318.
  • 2[2]Coucke P, Van Camp G, Djoyodiharjo B, et al. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families. N Engl J Med, 1994, 331: 425-431.
  • 3[3]Kubisch C, Schroeder BC, Friedrich T, et al. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell, 1999, 96: 437-446.
  • 4[4]Xia J-H, Liu C-Y, Tang B-S, et al. Mutations in the gene encoding gap junction protein a-3 associated with autosomal dominant hearing impairment. Nat Genet, 1998, 20:370-373.
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