A unique electrophoretic slow-moving glucose 6-phosphate dehydrogenase variant (G6PD Asahikawa) with a markedly acidic pH optimum

Author:

Takizawa T.,Fujii H.,Takegawa S.,Takahashi K.,Hirono A.,Morisaki T.,Kanno H.,Oka R.,Yoshioka H.,Miwa S.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference19 articles.

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

2. Beutler E, Yoshida A (1973) Human glucose-6-phosphate dehydrogenase variants: a supplementary tabulation. Ann Hum Genet 37:151?155

3. Beutler E, Mathai CK, Smith JE (1968) Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease. Blood 31:131?150

4. Beutler E, Matsumoto F, Daiber A (1974) Nonspherocytic hemolytic anemia due to G-6-PD Panama. IRCS 2:1389

5. Busch D, Boie K (1970) Glucose-6-Phosphat-Dehydrogenase-Defekt in Deutschland. II. Eigenschaften des Enzyms (Typ ?Freiburg?). Klin Wochenschr 18:74?78

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