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遗传性血管性水肿新的基因突变 被引量:1

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作者 汤蕊 张宏誉
出处 《中国医学科学院学报》 CAS CSCD 北大核心 2009年第6期734-,共1页 Acta Academiae Medicinae Sinicae
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  • 3Agostoni A,Cicardi M.Hereditary and acquired C1-inhibitor deficiency:biological and clinical characteristics in 235 patients[J].Medicine,1992,71:206-215.
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  • 5Iwamoto K,Mihara S,Ikezawa Z,et al.National prevalence survey of hereditary angioedema in Japan[J].Arerugi,2011,60:26-32.
  • 6Gompels MM,Lock RJ,Abinun M,et al.C1 inhibitor deficiency:consensus document[J].Clin Exp Immunol,2005,3:379-94.
  • 7Dewald G,Bork K.Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor[J].Biochem Biophys Res Commun,2006,4:1286-1289.
  • 8Bork K,Wulff K,Meinke P,et al.A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor[J].Clin Immunol,2011,1:31-35.
  • 9Lajos Kalmar.HAEdb C1 inhibitor gene mutation database[EB/OL].(2013-02)[2013-02-05].http://hae.enzim.hu/.
  • 10Xu YY,Zhi YX,Yin J,et al.Mutational spectrum and geno-phenotype correlation in Chinese families with Hereditary Angioedema[J].Allergy,2012,11:1430-1436.

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