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COCH基因与DFNA9的相关性研究 被引量:2

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出处 《吉林医学》 CAS 2007年第2期169-171,共3页 Jilin Medical Journal
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参考文献21

  • 1Hu Y.The genetics study of COCH gene and nonsyndromic hearing impairment[J].Audio and Spee Patho,2006,14:147.
  • 2Fransen E,Van Camp G.The COCH gene:a frequent cause of hearing impairment and vestibular dysfunction ?[J].Br J Audiol,1999,33 (5):297.
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  • 4Robertson NG,Skvorak AB,Yin Y,et al.Mapping and characterization of a novel cochlear gene in human and in mouse:a positional candidate gene for a deafness disorder,DFNA9[J].Genomics,1997,46 (3):345.
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同被引文献42

  • 1赵苏瑛,张海军,徐春宏,单云峰,单祥年,史庭燕.非综合征耳聋大家系永生细胞系的建立及几种EB病毒转化外周血淋巴细胞建系方法的探讨[J].遗传,2005,27(3):447-450. 被引量:12
  • 2孙悍军,陶然,程静,杨淑芝,曹菊阳,于黎明,洪梦迪,冯国鄞,戴朴,袁慧军,韩东一,贺林.常染色体显性遗传非综合征型耳聋致病基因定位研究[J].遗传,2006,28(12):1489-1494. 被引量:2
  • 3Shastry BS. SNP alleles in human disease and evolution[J]. J Hum Genet, 2002, 47 (11) : 561-566.
  • 4Shen LX, Basilion JP, StantonVP, et al. Single-nucleotide polymorphisms can cause different structural folds of mRNA[J]. Proc Natl Acad Sci USA, 1999, 96 (14) : 7871- 7876.
  • 5Kruglyak L, Nickerson DA. Variation is the spice of life[J]. Nat Genet, 2001, 27 (3) : 234-236.
  • 6Werner M, Herbon N, Gohlke H, et al. Asthma is associated with single-nucleotide polymorphisms in ADAM33[J]. Clin Exp Allergy, 2004, 34 (1) : 26-31.
  • 7Guo J, Cooper LF. Influence of an LRP5 cytoplasmic SNP on Wnt signaling and osteoblastic differentiation[J]. Bone, 2007, 40 (1) : 57-67.
  • 8Kubo M, Hata J, Ninomiya T, et al. A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction[J]. Nat Genet, 2007, 39 (2) : 212-217.
  • 9Seki S, Kawaguchi Y, Chiba K, et al. A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease[J]. Nat Genet, 2005, 37 (6) : 607-612.
  • 10Yang JW, Jang WS, Hong SD, et al. A case-control association study of the polymorphism at the promoter region of the DRD4 gene in Korean boys with attention deficit-hyperactivity disorder: evidence of association with the -521 C/T SNP[J]. Prog Neuropsychopharmacol Biol Psychiatry, 2008, 32 (1): 243 -248.

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