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Cytochrome b5 reductase deficiency and hereditary methemoglobinemia

Bibliographic Details
Main Author: Reading, Scott
Format: eBook
Language:English
Published: London Henry Stewart Talks 2018, 2018
Series:Protein epidemiology : understanding human diseases at the level of protein structure and function
Subjects:
Diagnosis, Differential
Methemoglobinemia / Congenital
Phenotype
Genetic Disorders
Methemoglobinemia
Methemoglobinemia / Diagnosis
Cytochrome-b(5) Reductase / Deficiency
Mutation
Methemoglobinemia / Therapy
Online Access:
Collection: Henry Stewart Talks - Collection details see MPG.ReNa
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300 |a 1 online resource (1 streaming video file (26 min.)  |b color, sound) 
505 0 |a 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 
653 |a Diagnosis, Differential 
653 |a Methemoglobinemia / congenital 
653 |a Phenotype 
653 |a Genetic disorders 
653 |a Methemoglobinemia 
653 |a Methemoglobinemia / diagnosis 
653 |a Cytochrome-B(5) Reductase / deficiency 
653 |a Mutation 
653 |a Methemoglobinemia / therapy 
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