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PMID: 5723728 Published · ppublish English Journal Article

Differences between alpha- and beta-chain mutants of human haemoglobin and between alpha- and beta-thalassaemia. Possible duplication of the alpha-chain gene.

British medical journal ·Vol. 4 ·No. 5633 ·1968-12-21 ·Pages 748-50

Lehmann H, Carrell RW

Abstract

Human adult haemoglobin consists of two unlike pairs of polypeptide chains, and can be described as alpha(2)beta(2). Amino-acid substitutions in either of the two types of chain result in alpha- and beta-chain variants. In thalassaemia, which causes a lowered production of haemoglobin, the alpha or the beta chain can be affected, the result being alpha- or beta-thalassaemia. There is a quantitative difference in the proportion of alpha- and beta-chain variants to normal haemoglobin in the respective heterozygotes, and there is also a difference in the pattern of inheritance of alpha- and beta-thalassaemia: these could possibly be explained by assuming that man has one gene for the beta- and two for the alpha-chain.

MeSH Terms
Hemoglobins/biosynthesis,isolation & purification Hemoglobins, Abnormal Humans Molecular Biology Mutation Thalassemia/genetics
Chemicals
Hemoglobins Hemoglobins, Abnormal
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lehmann H
Carrell R W
References (11)
11 references, click to expand
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Article Info
Journal
British medical journal
Abbr.
Br Med J
ISSN
0007-1447
Published
1968-12-21
Pages
748-50
Language
English
Region
England
NLM ID
0372673
PMCID
PMC1912890
Subset
IM
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