Phosphoglycerate kinase: an X-linked polymorphism in man.

American journal of human genetics ·Vol. 23 ·No. 1 ·1971-01-00 ·Pages 87-91

Chen SH, Malcolm LA, Yoshida A, Giblett ER

Abstract

暂无摘要

MeSH Terms

Electrophoresis Erythrocytes/enzymology Female Genetic Linkage Glycerophosphates Humans Male New Guinea Pedigree Phosphotransferases/blood Polymorphism, Genetic Sex Chromosomes

Chemicals

Glycerophosphates Phosphotransferases

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Chen S H

Malcolm L A

Yoshida A

Giblett E R

References (5)

5 references, click to expand

Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia.
Biochem Biophys Res Commun. 1968 Jan 25;30(2):173-7 PMID: 4230542
Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome.
N Engl J Med. 1969 Mar 6;280(10):528-34 PMID: 5764452
Crystalline 3-phosphoglycerate kinase from skeletal muscle.
Biochem J. 1969 Jul;113(3):551-4 PMID: 5807214
Electrophoresis of phosphoglycerate kinase.
Biochem Genet. 1969 Apr;3(2):189-95 PMID: 5364926
DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS.
Proc Natl Acad Sci U S A. 1963 Sep;50:481-5 PMID: 14067093

Article Info

Journal

American journal of human genetics

Abbr.

Am J Hum Genet

ISSN

0002-9297

Published

1971-01-00

Pages

87-91

Language

English

Region

United States

NLM ID

0370475

PMCID

PMC1706635

Subset

External Links

PubMed source PMC Full Text View journal details

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