The molecular basis for genetic deficiency of the second component of human complement
about
Infectious diseases associated with complement deficiencies.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)Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus. Results of a multicenter studyComplement in the pathophysiology and diagnosis of human diseases.Defect of a complement receptor 3 epitope in a patient with systemic lupus erythematosus.Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.Rare autoimmune disorders with Mendelian inheritance.
P2860
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P2860
The molecular basis for genetic deficiency of the second component of human complement
description
1985 nî lūn-bûn
@nan
1985 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1985 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
name
The molecular basis for genetic deficiency of the second component of human complement
@ast
The molecular basis for genetic deficiency of the second component of human complement
@en
The molecular basis for genetic deficiency of the second component of human complement
@nl
type
label
The molecular basis for genetic deficiency of the second component of human complement
@ast
The molecular basis for genetic deficiency of the second component of human complement
@en
The molecular basis for genetic deficiency of the second component of human complement
@nl
prefLabel
The molecular basis for genetic deficiency of the second component of human complement
@ast
The molecular basis for genetic deficiency of the second component of human complement
@en
The molecular basis for genetic deficiency of the second component of human complement
@nl
P2093
P1476
The molecular basis for genetic deficiency of the second component of human complement
@en
P2093
A S Whitehead
H R Colten
H S Auerbach
P Kilbridge
P356
10.1056/NEJM198507043130103
P407
P577
1985-07-04T00:00:00Z