Two cases of glucose-6-phophate dehydrogenase-deficient Nepalese belonging to the G6PD Mediterranean-type, not India-Pakistan sub-type but Mediterranean-Middle East sub-type

Author:

Matsuoka Hiroyuki,Jichun Wang,Hirai Makoto,Yoshida Shigeto,Arai Meiji,Ishii Akira,Baral Madhav Prasad

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. 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

2. Chen EY, Cheng A, Lee A, Kuang WJ, Hillier L, Green P, Schlessinger D, Ciccodicola A, D'Urso M (1991) Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome. Genomics 10:792–800

3. Fujii H, Miwa S (1998) Red blood cell enzymes and their clinical application. Adv Clin Chem 33:1-54

4. Fujii H, Takahashi K, Miwa S (1984) A new simple screening method for glucose 6-phosphate dehydrogenase deficiency. Acta Haematol Jpn 47:185–188

5. Henderson A, Baronne A (1987) Glucose-6-phosphate dehydrogenase deficiency in healthy Nepalese patients. Trans Roy Soc Trop Med Hyg 81:543

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