Congenital methemoglobinemia due to diaphorase deficiency.

Ozsoylu, S

Ozsoylu, S.

Acta Haematol ; 47(3): 175-81, 1972.

Article in En | MEDLINE | ID: mdl-4624255

Subject(s)

Dihydrolipoamide Dehydrogenase/blood; Metabolism, Inborn Errors; Methemoglobinemia/genetics; Child, Preschool; Electrophoresis; Erythrocytes/enzymology; Genes, Recessive; Glucosephosphate Dehydrogenase/blood; Glutathione/blood; Humans; Intellectual Disability/etiology; Male; Metabolism, Inborn Errors/complications; Metabolism, Inborn Errors/genetics; Methemoglobinemia/etiology; Quinones/urine; Spectrophotometry

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Collection: 01-internacional Database: MEDLINE Main subject: Dihydrolipoamide Dehydrogenase / Metabolism, Inborn Errors / Methemoglobinemia Type of study: Etiology_studies Limits: Child, preschool / Humans / Male Language: En Journal: Acta Haematol Year: 1972 Document type: Article

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