Molecular heterogeneity underlying the G6PD Mediterranean phenotype

Author:

Corcoran C. M.,Calabrò V.,Tamagnini G.,Town M.,Haidar B.,Vulliamy T. J.,Mason P. J.,Luzzatto L.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Beutler E (1983) Glucose-6-phosphate dehydrogenase deficiency. In: Stanbury JB, Wyngaarden JB, Fredrickson DS, Goldstein JL, Brown MS (eds) The metabolic basis of the inherited diseases, 5th edn. McGraw-Hill, New York, pp 1629–1653

2. Beutler E (1991) Glucose-6-phosphate dehydrogenase deficiency. N Engl J Med 324:169–174

3. Beutler E, Kuhl W (1990) The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia. Am J Hum Genet 47:1008–1012

4. Beutler E, Kuhl W, Gelbart T, Forman L (1991) DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants. J Biol Chem 266:4145–4150

5. Calabrò V, Giacobbe A, Vallone D, Montanaro V, Cascone A, Filosa S, Battistuzzi G (1990) Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in Southern Italy: a study on a population from the Matera district. Hum Genet 86:49–53

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