Cytochrome b5 reductase deficiency and hereditary methemoglobinemia [electronic resource] / Scott Reading.
Material type:
FilmSeries: Henry Stewart talksBiomedical & life sciences collection. Protein epidemiology: Publisher: London : Henry Stewart Talks, 2018Description: 1 online resource (1 streaming video file (26 min.) : color, sound)Subject(s): Genetic disorders | Methemoglobinemia | Cytochrome-B(5) Reductase -- deficiency | Diagnosis, Differential | Methemoglobinemia -- congenital | Methemoglobinemia -- diagnosis | Methemoglobinemia -- therapy | Mutation | PhenotypeOnline resources: Click here to access online | Series Animated audio-visual presentation with synchronized narration.
Title from title frames.
Contents: Formation of methemoglobinemia -- Review of methemoglobinemias types -- Cytochrome b5 reductase (Cytb5 R) -- Mutations and clinical phenotypes of Cytb5 R deficiency -- Differential diagnosis from other methemoglobinemias -- Therapy of methemoglobinemia.
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Mode of access: World Wide Web.