A case of hereditary methemoglobinemia with NADH-methemoglobin reductase (diaphorase) deficiency.

Patel, K C; Dudani, R A; Dalvi, S G; Dastur, F D; Acharya, V N; Bapat, J P; Baxi, A J; Kulkarni, K V; Sukumaran, P K

Patel, K C; Dudani, R A; Dalvi, S G; Dastur, F D; Acharya, V N; Bapat, J P; Baxi, A J; Kulkarni, K V; Sukumaran, P K.

Article in English | IMSEAR | ID: sea-22117

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Adolescent; Adult; Child; Female; Humans; Male; Methemoglobin; Methemoglobinemia/enzymology; NADH, NADPH Oxidoreductases/deficiency

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Female / Humans / Male / Methemoglobin / Child / Adolescent / Adult / Methemoglobinemia / NADH, NADPH Oxidoreductases Language: English Year: 1974 Type: Article

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