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感音神经性聋分子生物学研究进展 被引量:3

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作者 罗伟 孙建军
出处 《听力学及言语疾病杂志》 CAS CSCD 2003年第4期303-305,共3页 Journal of Audiology and Speech Pathology
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  • 1Hmani M, Ghorbel A, Boulila Elgaied A, et al. A novel locus for Usher syndrome type Ⅱ, USH2B,maps to chromosome 3 at p23 - 24.2[J].Eur J Hum Genet, 1999,7:363.
  • 2Gasparini P, Estivill X, Fortina P. Vestibular and hearing loss in genetic and metabolic disorder[J]. Curr Opin Neurol, 1999,12:35.
  • 3Kubisch C,Schroeder BC, Friedrich T, et al. KCNQ4, anovel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness[J]. Cell, 1999,96:437.
  • 4Hasson T, Heintzelman MB, Santos Sacchi J, et al. Expression in cochlear and retino of myosin Ⅶa, the gene product defective in Usher syndrome type 1B[J] .Proc Natl Acad Sci USA, 1995,92:9 815.
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  • 7Fukushima K, Kasai N, Ueki Y, et al. A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23 - 24.3[J]. Am J Hum Genet, 1999,65: 141.
  • 8Seidman MD. Effects of dietary restricifion and anfioxidiants on presbyacusis[J]. Laryngoscope, 2000,110:727.
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