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Article

Molecular genetics of glucose-6-phosphate dehydrogenase deficiency in Mexico.

Blood cells, molecules & diseases - 1 Jan 1997

Medina M D, Vaca G, Lopez-Guido B, Westwood B, Beutler E

Abstract excerpt

Several studies carried out between 1965 and 1985 showed that G-6-PD deficiency in Mexico is heterogeneous at the biochemical level and that the G-6-PD A- phenotype is relatively common. We have now investigated the molecular basis of G-6-PD deficiency in Mexico. Up-to-date 60 chromosomes with G6PD mutations have been studied, 16 in previous studies and 44 in the present work. Molecular analysis of DNA from...

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Identifiers

PMID: 9215753
DOI: 10.1006/bcmd.1997.0124

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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