Maternal 3-methylglutaconic aciduria associated with abnormalities in offspring

Author:

de Koning TJ,Duran M,Dorland L,Berger R,Poll-The BT

Publisher

Elsevier BV

Subject

General Medicine

Reference5 articles.

1. Multiple syndromes of 3-methylglutaconic aciduria;Gibson;Pediatr Neurol,1993

2. 3-methylglutaconic acidemia in Smith-Lemli-Opitz syndrome;Kelley;Pediatr Res,1995

3. Inherited 3-methylglutaconic aciduria in two brothers: another defect of leucine metabolism;Duran;J Pediatr,1982

4. Branched-chain organic acidurias;Ogier de Baulny,1995

5. 3-methylglutaconic aciduria in two adults;Kuhara;Clin chim Acta,1992

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1. Maladies héréditaires du métabolisme;Le diagnostic prénatal en pratique;2011

2. The 3-methylglutaconic acidurias: what’s new?;Journal of Inherited Metabolic Disease;2010-09-30

3. Case Report: 3-Methyglutaconic Aciduria in a Chinese Patient with Glycogen Storage Disease Ib;Journal of Inherited Metabolic Disease;2003-10

4. High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased Km): relevance to genetic disease and polymorphisms;The American Journal of Clinical Nutrition;2002-04-01

5. What is the origin of 3-methylglutaconic acid?;Journal of Inherited Metabolic Disease;1999-05

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