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PMID: 6480834 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigens.

The Journal of clinical investigation ·Vol. 74 ·No. 4 ·1984-10-00 ·Pages 1509-14

Muir WA, Hedrick S, Alper CA, Ratnoff OD, Schacter B, Wisnieski JJ

Abstract

We have studied a family in which the proband had systemic lupus erythematosus and selective incomplete deficiency of the fourth component of complement (C4) (2-5% of the normal level). An additional six healthy family members also had low C4 levels (2.4-24.1% of normal) but no evidence of lupus. This form of inherited C4 deficiency differs from that in previously reported families in that inheritance was autosomal dominant (rather than recessive), C4 levels were markedly reduced (but not undetectable), and there was no linkage to HLA, BF, or C4 structural loci, all known to be within the major histocompatibility complex.

MeSH Terms
Adult Complement C4/deficiency,genetics,immunology Female Genes, Dominant Genetic Linkage Hemolysis Humans Isoantigens/analysis Lupus Erythematosus, Systemic/genetics,immunology Major Histocompatibility Complex Pedigree
Chemicals
Complement C4 Isoantigens
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Muir W A
Hedrick S
Alper C A
Ratnoff O D
Schacter B
Wisnieski J J
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28 references, click to expand
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1984-10-00
Pages
1509-14
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC425321
Subset
IM
Grants
NIAID NIH HHS · AI-14157 · United States
NHLBI NIH HHS · HL-01661 · United States
NCRR NIH HHS · RR00080 · United States
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