Single nucleotide polymorphism in CPT1B and CPT2 genes and its association with blood carnitine levels in acute myocardial infarction patients
Author:
Funder
National Plan for Science and Technology (NPST) Program by King Saud University
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference31 articles.
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3. Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency;Bennett;Mol. Genet. Metab.,2004
4. Carnitine;Bieber;Annu. Rev. Biochem.,1988
5. Carnitine uptake into human heart cells in culture;Bohmer;Biochim. Biophys. Acta,1977
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