A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity.
第一作者:
Anna M,Blom
第一单位:
Lund University, Department of Laboratory Medicine, Malmö University Hospital, Malmö, Sweden.
作者:
主题词
急性肾损伤(Acute Kidney Injury);青少年(Adolescent);成年人(Adult);氨基酸取代(Amino Acid Substitution);儿童(Child);队列研究(Cohort Studies);补体C4b结合蛋白质(Complement C4b-Binding Protein);补体因子H(Complement Factor H);补体途径, 旁路(Complement Pathway, Alternative);女(雌)性(Female);基因表达调控(Gene Expression Regulation);溶血尿毒症综合征(Hemolytic-Uremic Syndrome);杂合子(Heterozygote);组织相容性抗原(Histocompatibility Antigens);人类(Humans);男(雄)性(Male);中年人(Middle Aged);多态现象, 遗传(Polymorphism, Genetic)
DOI
10.4049/jimmunol.180.9.6385
PMID
18424762
发布时间
2019-05-16
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