Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase.

M.J. Percy, L.J. Crowley, C.A. Davis, Mary McMullin, G. Savage, J. Hughes, C. McMahon, R.J. Quinn, O. Smith, M.J. Barber, Terence Lappin

Research output: Contribution to journalArticle

14 Citations (Scopus)
Original languageEnglish
Pages (from-to)847-853
Number of pages7
JournalBritish Journal of Haematology
Volume129(6)
Issue number6
DOIs
Publication statusPublished - Jun 2005

ASJC Scopus subject areas

  • Hematology

Cite this

Percy, M. J., Crowley, L. J., Davis, C. A., McMullin, M., Savage, G., Hughes, J., McMahon, C., Quinn, R. J., Smith, O., Barber, M. J., & Lappin, T. (2005). Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase. British Journal of Haematology, 129(6)(6), 847-853. https://doi.org/10.1111/j.1365-2141.2005.05526.x