G6PD mahidol, a common deficient variant in South East Asia is caused by a (163)glycine----serine mutation.

Nucleic acids research ·Vol. 17 ·No. 14 ·1989-07-25 ·Pages 5868

Vulliamy TJ, Wanachiwanawin W, Mason PJ, Luzzatto L

Abstract

暂无摘要

MeSH Terms

Asia, Southeastern Base Sequence Genes Genetic Variation Glucosephosphate Dehydrogenase/genetics Glucosephosphate Dehydrogenase Deficiency/genetics Glycine Humans Molecular Sequence Data Mutation Serine

Chemicals

Serine Glucosephosphate Dehydrogenase Glycine

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Vulliamy T J

Department of Haematology, Hammersmith Hospital, London, UK.

Wanachiwanawin W

Mason P J

Luzzatto L

References (2)

2 references, click to expand

Glucose-6-phosphate dehydrogenase deficiency. Part 2. Tropical Asia.
Clin Haematol. 1981 Oct;10(3):800-14 PMID: 7030553
Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.
Proc Natl Acad Sci U S A. 1988 Jul;85(14):5171-5 PMID: 3393536

Article Info

Journal

Nucleic acids research

Abbr.

Nucleic Acids Res

ISSN

0305-1048

DOI

10.1093/nar/17.14.5868

Published

1989-07-25

Pages

5868

Language

English

Region

England

NLM ID

0411011

PMCID

PMC318229

Subset

External Links

PubMed source DOI: 10.1093/nar/17.14.5868 PMC Full Text View journal details

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G6PD mahidol, a common deficient variant in South East Asia is caused by a (163)glycine----serine mutation.

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