Carnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and Nunavut-Reference-Cited by-同舟云学术

Carnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and Nunavut

Published:2010-10 Issue:2-3 Volume:101 Page:200-204
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Collins Sorcha A.,Sinclair Graham,McIntosh Sarah,Bamforth Fiona,Thompson Robert,Sobol Isaac,Osborne Geraldine,Corriveau Andre,Santos Maria,Hanley Brendan,Greenberg Cheryl R.,Vallance Hilary,Arbour Laura

Funder

CIHR

Michael Smith Foundation for Health Research Scholar

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference23 articles.

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2. Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency;Bougnères;J. Pediatr.,1981

3. A possible role for malonyl-CoA in the regulation of hepatic fatty acid oxidation and ketogenesis;McGarry;J. Clin. Invest.,1977

4. Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program;Prasad;Mol. Genet. Metab.,2001

5. The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis;McGarry;Eur. J. Biochem.,1997

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