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Title: Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type. Author: Kahn A, Marie J, Desbois JC, Boivin P. Journal: Acta Haematol; 1976; 56(1):58-64. PubMed ID: 822676. Abstract: In a Portuguese boy with favism G-6PD deficiency was found. Deficiency was due to a G-6PD variant close or identical to Canton-type G-6PD. The muted protein had a lowered catalytic activity and furthermore, was unstable. The post-translational modifications undergone by this deficient G-6PD variant are described.[Abstract] [Full Text] [Related] [New Search]