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PMID: 3338798 Published · ppublish English Case Reports Journal Article

G6PD Viangchan: a new glucose 6-phosphate dehydrogenase variant from Laos.

Human genetics ·Vol. 78 ·No. 1 ·1988-01-00 ·Pages 98-9

Poon MC, Hall K, Scott CW, Prchal JT

Abstract

We describe a previously unreported glucose-6-phosphate dehydrogenase-(G6PD) variant. G6PD Viangchan was found in a Laotian immigrant to Calgary, Canada, and was characterized by severe enzyme deficiency, normal electrophoretic mobility, increased pH optimum, and abnormal kinetics for the natural substrates G6PD and NADP, as well as the artificial substrates 2-deoxy G6PD and deamino NADP. The inhibition constant for NADPH was decreased. The subject has no evidence suggesting chronic or episodic hemolysis.

MeSH Terms
Child Genetic Variation Glucosephosphate Dehydrogenase/genetics Humans Kinetics Laos Male
Chemicals
Glucosephosphate Dehydrogenase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Poon M C
Division of Hematology, University of Calgary, Alberta, Canada.
Hall K
Scott C W
Prchal J T
References (5)
5 references, click to expand
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    Blood. 1968 Feb;31(2):131-50 PMID: 5643703
  2. Hemolytic anemia and G6PD deficiency.
    Science. 1973 Feb 9;179(4073):532-7 PMID: 4405605
  3. G-6-PD variants in Chinese in Thailand.
    Southeast Asian J Trop Med Public Health. 1980 Jun;11(2):250-5 PMID: 7434076
  4. Embryonic zeta-globin chains in adults: a marker for alpha-thalassemia-1 haplotype due to a greater than 17.5-kb deletion.
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  5. The removal of leukocytes and platelets from whole blood.
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1988-01-00
Pages
98-9
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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