Distribution and Heredity of Erythrocyte G6PD Activity and Electrophoretic Variants Among Different Racial Groups at São Paulo, Brazil

Overview

Journal J Med Genet

Specialty Genetics

Date 1969 Mar 1

PMID 5771222

Citations 6

Authors

P H Saldanha

F G Nobrega

J C Maia

Affiliations

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Citing Articles

Late-Life Presentation of Unsuspected G6PD Deficiency.

Benchimol M, Madeira L, de Oliveira-Souza R Case Rep Crit Care. 2018; 2018:8198565.

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G6PD deficiency in Latin America: systematic review on prevalence and variants.

Monteiro W, Val F, Siqueira A, Franca G, Sampaio V, Melo G Mem Inst Oswaldo Cruz. 2014; 109(5):553-68.

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Genetic studies on southeastern Bantu of Mozambique. I. Variants of glucose-6-phosphate dehydrogenase.

REYS L, Manso C, Stamatoyannopoulos G Am J Hum Genet. 1970; 22(2):203-15.

PMID: 5435642 PMC: 1706530.

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.

Zatz M, Itskan S, SANGER R, FROTA-PESSOA O, Saldanha P J Med Genet. 1974; 11(4):321-7.

PMID: 4548443 PMC: 1013198. DOI: 10.1136/jmg.11.4.321.

X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg.

Zatz M, Otto P J Med Genet. 1976; 13(3):217-22.

PMID: 1084423 PMC: 1013396. DOI: 10.1136/jmg.13.3.217.

References

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