Complement-human histocompatibility antigen haplotypes in C2 deficiency.
about
Type II human complement C2 deficiency. Allele-specific amino acid substitutions (Ser189 --> Phe; Gly444 --> Arg) cause impaired C2 secretionInfectious diseases associated with complement deficiencies.Complement factor 2 deficiency: a clinical and serological family studyComplete complement deficiency in a large cohort of familial systemic lupus erythematosus.Links between complement abnormalities and systemic lupus erythematosus.A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes)Genetic deficiencies of complement.
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P2860
Complement-human histocompatibility antigen haplotypes in C2 deficiency.
description
1981 nî lūn-bûn
@nan
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
1981年论文
@zh
1981年论文
@zh-cn
name
Complement-human histocompatibility antigen haplotypes in C2 deficiency.
@en
type
label
Complement-human histocompatibility antigen haplotypes in C2 deficiency.
@en
prefLabel
Complement-human histocompatibility antigen haplotypes in C2 deficiency.
@en
P2093
P2860
P356
P1476
Complement-human histocompatibility antigen haplotypes in C2 deficiency.
@en
P2093
E W Gelfand
R B Johnston
P2860
P304
P356
10.1172/JCI110070
P407
P577
1981-02-01T00:00:00Z