A carregar...

Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.

Glutaric acidemia type II (GA II) is a human genetic disorder. It has been suggested that the primary defect in this disorder is a deficiency of a protein involved in electron transport between the acyl-CoA dehydrogenases and the bc1 complex of the mitochondrial respiratory chain. Antisera were rais...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Frerman, F E, Goodman, S I
Formato: Artigo
Idioma:Inglês
Publicado em: 1985
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC391133/
https://ncbi.nlm.nih.gov/pubmed/2989828
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!