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国内聋病基因研究取得新进展 被引量:6

Recent advances in genetic research on hereditary deafness
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作者 杨伟炎
出处 《中华耳科学杂志》 CSCD 2005年第4期239-240,共2页 Chinese Journal of Otology
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  • 2王秋菊,李庆忠,刘穹,郭维,顾瑞,杨伟炎,王荣光,沈岩,韩东一.遗传性听神经病的基因定位及候选基因筛查研究[J].中华耳科学杂志,2005,3(4):245-252. 被引量:12
  • 3戴朴,黄德亮,王嘉陵,冯勃,翟所强,康东洋,张昕,刘新,曹菊阳,李梅,刘丽贤,袁慧军.PDS基因检测—诊断大前庭水管综合征的新方法[J].中华耳科学杂志,2005,3(4):241-244. 被引量:19
  • 4赵亚丽,翟所强,王秋菊.大前庭水管综合征及其相关的基因—SLC26A4[J].中华耳科学杂志,2005,3(4):289-292. 被引量:10
  • 5[6]Li Z,Li R,Chen J,et al.Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycosideinduced and non-syndromic hearing loss.Human Genetics,2005,117:9-15.
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  • 7[8]Zhao LD,Young WY,Li R,et al.Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.Biochem Biophys Res Commun.2004,325:1503-1508.
  • 8[9]Zhao H,Young WY,Yan Q,et al.Functional characterization of the mitochondrial 12S rRNA C 1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss.NucleicAcids Research,2005,33:1132-1139.
  • 9[10]Prezant TR,Agapian JV,Bohlman MC,et al.Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.Nature Genetics,1993,4:289-294.
  • 10[11]van den Ouweland JM,Lemkes HH,Gerbitz KD,et al.Maternally inherited diabetes and deafness (MIDD) :a distinct subtype ofdiabetes associated with a mitochondrial tRNALeu (UUR) gene point mutation.Muscle and Nerve,1995,3:S124-130.

二级参考文献68

共引文献46

同被引文献56

  • 1赵世巧,冯文莉.基因治疗的病毒载体研究进展[J].国外医学(临床生物化学与检验学分册),2005,26(10):709-711. 被引量:15
  • 2李晨,安云庆.腺相关病毒载体及其在基因治疗中的应用[J].中国康复理论与实践,2006,12(1):51-52. 被引量:3
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