Literature DB >> 9156317

Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Poland--a study on the 563 and 1311 mutations of the G6PD gene.

E Jabłońska-Skwiecińska1, J G Zimowski, J Kłopocka, M Bisko, D Hoffman-Zacharska, J Zaremba.   

Abstract

Studies on the mutation 563T and silent mutation 1311T of the glucose-6-phosphate dehydrogenase (G6PD) gene in Poland were performed in 26 families affected with G6PD deficiency classified-according to WHO-as group 2 G6PD deficiency. Both mutations were found in 19 families, including 17 of Polish origin. Mutation 563T alone was found in 1 Greek female. The frequency of the silent mutation 1311T in Polish unaffected controls was 0.10. It is postulated that at least parts of the Polish (or Middle-Eastern European) and Mediterranean populations are of a common origin.

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Year:  1997        PMID: 9156317

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  2 in total

1.  Glucose-6-phosphate dehydrogenase (G6PD) mutations and haemoglobinuria syndrome in the Vietnamese population.

Authors:  Nguyen Thi Hue; Jean Paul Charlieu; Tran Thi Hong Chau; Nick Day; Jeremy J Farrar; Tran Tinh Hien; Sarah J Dunstan
Journal:  Malar J       Date:  2009-07-10       Impact factor: 2.979

2.  Three-dimensional modeling of glucose-6-phosphate dehydrogenase-deficient variants from German ancestry.

Authors:  Farooq Kiani; Sonja Schwarzl; Stefan Fischer; Thomas Efferth
Journal:  PLoS One       Date:  2007-07-18       Impact factor: 3.240

  2 in total

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