TY  - ADVS
AU  - Reading,Scott
TI  - Cytochrome b5 reductase deficiency and hereditary methemoglobinemia
T2  - Protein epidemiology : understanding human diseases at the level of protein structure and function,
PY  - 2018///
CY  - London
PB  - Henry Stewart Talks
KW  - Genetic disorders
KW  - Methemoglobinemia
KW  - Cytochrome-B(5) Reductase
KW  - deficiency
KW  - Diagnosis, Differential
KW  - congenital
KW  - diagnosis
KW  - therapy
KW  - Mutation
KW  - Phenotype
N1  - 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; Access restricted to subscribers
UR  - https://hstalks.com/bs/3679/
UR  - https://hstalks.com/bs/p/33/
ER  -