Demonstration of an enzyme variant in a case of congenital methaemoglobinaemia.

British medical journal ·Vol. 4 ·No. 5573 ·1967-10-28 ·Pages 212-4

West CA, Gomperts BD, Huehns ER, Kessel I, Ashby JR

Abstract

暂无摘要

MeSH Terms

Blood Protein Electrophoresis Child Dihydrolipoamide Dehydrogenase/blood Hemoglobins/analysis Hemolysis Humans Male Methemoglobinemia/congenital,enzymology

Chemicals

Hemoglobins Dihydrolipoamide Dehydrogenase

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

West C A

Gomperts B D

Huehns E R

Kessel I

Ashby J R

References (3)

3 references, click to expand

Mental retardation in methemoglobinemia due to diaphorase deficiency.
N Engl J Med. 1965 Oct 14;273(16):840-5 PMID: 4378489
Erythrocyte metabolism. VI. Separation of erythrocyte enzymes from hemoglobin.
J Clin Invest. 1962 Jun;41:1257-62 PMID: 13906488
The relation of diaphorase of human erythrocytes to inheritance of methemoglobinemia.
J Clin Invest. 1960 Jul;39:1176-9 PMID: 14444209

Article Info

Journal

British medical journal

Abbr.

Br Med J

ISSN

0007-1447

DOI

10.1136/bmj.4.5573.212

Published

1967-10-28

Pages

212-4

Language

English

Region

England

NLM ID

0372673

PMCID

PMC1748606

Subset

External Links

PubMed source DOI: 10.1136/bmj.4.5573.212 PMC Full Text

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Demonstration of an enzyme variant in a case of congenital methaemoglobinaemia.

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