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Cytochrome b5 reductase deficiency and hereditary methemoglobinemia
Title
Cytochrome b5 reductase deficiency and hereditary methemoglobinemia [electronic resource] / Scott Reading.
Published
London : Henry Stewart Talks, 2018.
Physical Description
1 online resource (1 streaming video file (26 min.) : color, sound).
Local Notes
Access is available to the Yale community.
Notes
Animated audio-visual presentation with synchronized narration.
Title from title frames.
Access and use
Access restricted by licensing agreement.
Format
Images / Online / Video & Film
Language
English
Added to Catalog
April 09, 2018
Series
Protein epidemiology : understanding human diseases at the level of protein structure and function,
Contents
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.
Publisher's number
4275 Henry Stewart Talks
Subjects
Subjects (Medical)
Cytochrome-B(5) Reductase - deficiency.
Mutation.
Bookmark As
Citation
