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Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts.

Propionyl-CoA carboxylase (PCC) deficiency is an inherited metabolic disorder showing considerable variability of expression. We have investigated the possibility that there is a genetic basis for the clinical heterogeneity in this disorder by examining complementation in Sendai virus mediated heter...

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Detalhes bibliográficos
Main Authors: Gravel, R A, Lam, K F, Scully, K J, Hsia, Y
Formato: Artigo
Idioma:Inglês
Publicado em: 1977
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1685391/
https://ncbi.nlm.nih.gov/pubmed/195466
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