Literature DB >> 2220884

Congenital methemoglobinemia due to methemoglobin reductase deficiency in two unrelated American black families.

J T Prchal1, N Borgese, M R Moore, H Moreno, E Hegesh, M K Hall.   

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Year:  1990        PMID： 2220884     DOI： 10.1016/0002-9343(90)90384-p

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  2 in total

1.  Methemoglobin reductase activity and in vitro sensitivity towards oxidant induced methemoglobinemia in swiss mice and beagle dogs erythrocytes.

Authors:  S Srivastava; A S Alhomida; N J Siddiqi; S K Puri; V C Pandey
Journal:  Mol Cell Biochem       Date:  2002-03       Impact factor: 3.396

2.  A novel point mutation in a 3' splice site of the NADH-cytochrome b5 reductase gene results in immunologically undetectable enzyme and impaired NADH-dependent ascorbate regeneration in cultured fibroblasts of a patient with type II hereditary methemoglobinemia.

Authors:  K Shirabe; M T Landi; M Takeshita; G Uziel; E Fedrizzi; N Borgese
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025
  2 in total

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