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PMID: 848488 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Inheritance of low erythrocyte catechol-o-methyltransferase activity in man.

American journal of human genetics ·Vol. 29 ·No. 2 ·1977-03-00 ·Pages 125-35

Weinshilboum RM, Raymond FA

Abstract

Catechol-O-methyltransferase activity was measured in blood obtained from 373 randomly selected subjects aged 16-18, 262 consecutive adult blood donors, and 201 first-degree relatives of subjects with RBC COMT activity of less than 8 U. The distribution of RBC COMT activity in a randoly selected populations was apparently bimodal with a nadir at approximately 8 U. Of a randomly selected population, 23% had low RBC COMT activity (less than 8 U), Because of previous reports of a significant sibling-sibling correlation of RBC COMT activity and because of the presence of a subgroup of subjects with low enzyme activity, RBC COMT activity was measured in blood from first-degree relatives of probands with low erythrocyte enzyme activity in 48 families. The results of segregation analyses of the data were compatible with autosomal recessive inheritence of an allele for low RBC COMT activity. RBC COMT in blood samples from siblings of probands inthese families also showed an apparent biomodal distribution.

MeSH Terms
Adolescent Adult Blood Donors Catechol O-Methyltransferase/blood,deficiency Erythrocytes/enzymology Female Gene Frequency Genes, Recessive Humans Male Pedigree Sampling Studies
Chemicals
Catechol O-Methyltransferase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Weinshilboum R M
Raymond F A
References (12)
12 references, click to expand
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1977-03-00
Pages
125-35
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1685255
Subset
IM
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