The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations-Reference-Cited by-同舟云学术

The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations

Published:2009-04 Issue:4 Volume:96 Page:201-207
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Greenberg Cheryl R.,Dilling Louise A.,Thompson G. Robert,Seargeant Lorne E.,Haworth James C.,Phillips Susan,Chan Alicia,Vallance Hilary D.,Waters Paula J.,Sinclair Graham,Lillquist Yolanda,Wanders Ronald J.A.,Olpin Simon E.

Publisher

Elsevier BV

Subject

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

Reference44 articles.

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4. Hepatic and muscular presentations of carnitine palmitoyl transferase deficiency: two distinct entities;Demaugre;Pediatr. Res.,1988

5. Brief report: renal tubular acidosis in carnitine palmitoyltransferase type I deficiency;Falik-Borenstein;N. Engl. J. Med.,1992

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