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Enzyme deficiencies as the cause of hereditary nonspherocytic hemolytic anemia

✍ Scribed by A. Casado; Ma Casado; Ma R De la Torre; Ma E Lopéz-Fernandez; D. Carrascosa


Book ID
115090314
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
96 KB
Volume
42
Category
Article
ISSN
0009-9163

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## Communicated by Francesco Giannelli DNA sequencing revealed seven different glucose-6-phosphate dehydrogenase (G6PD) mutations in G6PD deficient subjects from 10 Polish families. Among them we found two novel mutations: 679C®T (G6PD Radlowo, class 2) and a 1006A®G (G6PD Torun, class 1). Variant