Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria-Reference-Cited by-同舟云学术

Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria

Published:2006-03 Issue:3 Volume:87 Page:219-225
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Lerner-Ellis Jordan P.,Gradinger Abigail B.,Watkins David,Tirone Jamie C.,Villeneuve Amélie,Dobson C. Melissa,Montpetit Alexandre,Lepage Pierre,Gravel Roy A.,Rosenblatt David S.

Publisher

Elsevier BV

Subject

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

Reference21 articles.

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2. The natural history of the inherited methylmalonic acidurias;Matsui;N. Engl. J. Med.,1983

3. Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria;Dobson;Hum. Mol. Genet.,2002

4. Genetic and biochemical analysis of human cobalamin mutants in cell culture;Fenton;Annu. Rev. Genet.,1978

5. MeaB is a component of the methylmalomyl-CoA mutase complex required for protection of the enzyme from inactivation;Korotkova;J. Biol. Chem.,2004

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