Maternal 3-methylglutaconic aciduria associated with abnormalities in offspring
Author:
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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