Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience-Reference-Cited by-同舟云学术

Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience

Published:2012-09 Issue:1-2 Volume:107 Page:72-80
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Kölker Stefan,Boy S.P. Nikolas,Heringer Jana,Müller Edith,Maier Esther M.,Ensenauer Regina,Mühlhausen Chris,Schlune Andrea,Greenberg Cheryl R.,Koeller David M.,Hoffmann Georg F.,Haege Gisela,Burgard Peter

Funder

Kindness-for-Kids Foundation

European Commission

Publisher

Elsevier BV

Subject

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

Reference71 articles.

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3. Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutations;Goodman;Hum. Mutat.,1998

4. Mutation analysis in glutaric aciduria type I;Zschocke;J. Med. Genet.,2000

5. Proton abstraction, steady-state kinetics, and oxidation–reduction potential of human glutaryl-CoA dehydrogenase;Dwyer;Biochemistry,2000

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