Carnitine palmitoyltransferase IA polymorphism P479L is common in Greenland Inuit and is associated with elevated plasma apolipoprotein A-I

Carnitine palmitoyltransferase IA, encoded by CPT1A, is a key regulator of fatty acid metabolism. Previously, a loss-of-function mutation, namely, c.1436 C→T (p.P479L), was reported in CPT1A in the homozygous state in Canadian aboriginal male with presumed CPT1A deficiency. To determine the populati...

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Detalhes bibliográficos
Main Authors: Rajakumar, Chandheeb, Ban, Matthew R., Cao, Henian, Young, T. Kue, Bjerregaard, Peter, Hegele, Robert A.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2009
Assuntos:
Patient-Oriented and Epidemiological Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2681405/
https://ncbi.nlm.nih.gov/pubmed/19181627
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.P900001-JLR200
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