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银屑病及Marie Unna遗传性稀毛症的遗传易感基因

Gene Mutations in Psoriasis and Marie Unna Hereditary Hypotrichosis
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摘要 1文献来源 [1] Zhang X J, Huang W, Yang S, et al. Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21 [J]. Nat Genet, 2009,41(2):205-210.
作者 王群 宗飒
出处 《循证医学》 CSCD 2009年第4期222-225,共4页 The Journal of Evidence-Based Medicine
关键词 银屑病 Marie Unna遗传性稀毛症 基因突变 psoriasis Marie Unna hereditary hypotrichosis gene mutations
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参考文献4

  • 1Bowcock AM, Cookson WO. The genetics of psoriasis, psoriatic arthritis and atopic dermatitis [J]. Hum Mol Genet, 2004, 13(1) :43-55.
  • 2Risch HA, Marrett LD, Jain M, et al. Differences in risk factors for epithelial ovarian cancer by histologic type. Results of a case-control study[J]. Am J Epidemiol, 1996, 144(4): 363-372.
  • 3van Steensel M, Smith FJ, Steijlen PM, et al. The gene for hypertrichosis of Marie Unna maps between D8S258 and D8S298: Exclusion of the hr gene by cDNA and genomic sequencing [J].Am J Hum Genet, 1999,65(2):413-419.
  • 4He PP, Zhang X J, Yang Q, et al. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3 [J]. Br J Dermatol, 2004, 150(5) :837-842.

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