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PMID: 722085 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

Evidence for a silent or null gene in hereditary C2 deficiency.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 121 ·No. 6 ·1978-12-00 ·Pages 2580-1

Pariser KM, Raum D, Berkman EM, Alper CA, Agnello V

Abstract

Three generations of a family with hereditary C2 deficiency were studied, Six members heterozygous for C2 deficiency were identified by serum C2 levels that were approximately 50% of normal C2 values and the identity was supported by HLA analysis. All six members with low C2 levels had only a single electrophoretic variant. Two of four children did not have the variant found in the parent from whom they inherited the partial C2 deficiency. It is inferred that the low levels of C2 result from the inheritance of a silent or null gene, C2D allelic with the structural genes controlling the electrophoretic variants.

MeSH Terms
Antigens Child, Preschool Complement C2/deficiency,genetics Female HLA Antigens/genetics Humans Isoelectric Focusing Pedigree
Chemicals
Antigens Complement C2 HLA Antigens
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Pariser K M
Raum D
Berkman E M
Alper C A
Agnello V
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1978-12-00
Pages
2580-1
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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