Impaired fasting tolerance among Alaska native children with a common carnitine palmitoyltransferase 1A sequence variant-Reference-Cited by-同舟云学术

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Impaired fasting tolerance among Alaska native children with a common carnitine palmitoyltransferase 1A sequence variant

Published:2011-11 Issue:3 Volume:104 Page:261-264
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Gillingham Melanie B.,Hirschfeld Matthew,Lowe Sarah,Matern Dietrich,Shoemaker James,Lambert William E.,Koeller David M.

Funder

National Institutes of Health

National Center for Research Resources (NCRR)

Publisher

Elsevier BV

Subject

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

Reference19 articles.

1. Molecular characterization of L-CPT I deficiency in six patients: insights into function of the native enzyme;Brown;J. Lipid Res.,2001

2. Prevalence and distribution of the c.1436C→T sequence variant of carnitine palmitoyltransferase 1A among Alaska Native infants;Gessner;J. Pediatr.,2011

3. The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations;Greenberg;Mol. Genet. Metab.,2009

4. Carnitine palmitoyltransferase IA polymorphism P479L is common in Greenland Inuit and is associated with elevated plasma apolipoprotein A-I;Rajakumar;J. Lipid Res.,2009

5. Carnitine Palmitoyltransferase 1A Deficiency;Bennett;Genereviews,2010

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