Heterogeneity in the genetic basis of human complement C9 deficiency

被引:12
作者
Witzel-Schlömp, K
Hobart, MJ
Fernie, BA
Orren, A
Würzner, R
Rittner, C
Kaufmann, T
Schneider, PM
机构
[1] Univ Mainz, Inst Legal Med, D-55131 Mainz, Germany
[2] MRC Ctr, Mol Immunopathol Unit, Cambridge, England
[3] Univ Coll, Dept Microbiol, Galway, Ireland
[4] Leopold Franzens Univ, Inst Hyg, Innsbruck, Austria
关键词
point mutations; hemolytic activity; ethnic origin;
D O I
10.1007/s002510050415
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
[No abstract available]
引用
收藏
页码:144 / 147
页数:4
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