NADH cytochrome b5 reductase activity in lymphoid cell lines. Expression of the defect in epstein Barr virus transformed lymphoblastoid cell lines from patients with recessive congenital methemoglobinemia.

Recessive congenital methemoglobinemia (RCM) is due to the homozygous deficiency of NADH-cytochrome b5 reductase (EC 1.6.2.2.). In type I disease, in which the patients are only methemoglobinemic, the enzyme defect is fully expressed in the erythrocytes, whereas the leukocytes are much less affected...

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Enregistré dans:
Détails bibliographiques
Auteurs principaux: Lostanlen, D, Lenoir, G, Kaplan, J C
Format: Artigo
Langue:Inglês
Publié: 1981
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC370795/
https://ncbi.nlm.nih.gov/pubmed/6265499
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