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Some Mexican glucose-6-phosphate dehydrogenase variants revisited

✍ Scribed by Ernest Beutler; Wanda Kuhl; Eva Ramirez; Ruben Lisker


Publisher
Springer
Year
1991
Tongue
English
Weight
369 KB
Volume
86
Category
Article
ISSN
0340-6717

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✦ Synopsis


Glucose-6-phosphate dehydrogenase (G6PD) deficiency appears to be fairly common in Mexico. We have now examined the DNA of three previously reported electrophoretically fast Mexican G6PD variants, -G6PD Distrito Federal, G6PD Tepic, and G6PD Castilla. All three of these variants, believed on the basis of biochemical characterization and population origin to be unique, have the G--~A transition at nucleotide 202 and the A---~G transition at nucleotide 376, mutations that we now recognize to be characteristic of G6PD A-. Two other Mexican males with G6PD deficiency were found to have the same mutation. All five have the (NlaIII! FokI/PvulI/PstI) haplotype characteristic of G6PD Ain Africa. Since the PvuII+ genotype seems to be rare in Europe, we conclude that all of these G6PD A-genes had their ancient origin in Africa, although in many of the Mexican patients with G6PD A -202A/376G the gene may have been imported more recently from Spain, where this variant, formerly known as G6PD Betica, is also prevalent.


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