Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference12 articles.
1. Defects of electron transfer flavoprotein and electron transfer flavoprotein–ubiquinone oxidoreductase: glutaric academia type II;Frerman,2001
2. Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency;Olsen;Hum. Mutat.,2003
3. Glutaric acidaemia type II (multiple acyl-Co-adehydrogenation deficiency;Goodman;J. Inherit. Metab. Dis.,1984
4. Electron transfer flavoprotein deficiency: functional and molecular aspects;Schiff;Mol. Genet. Metab.,2006
5. Glutaric acidemia type LL: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene;Goodman;Mol. Genet. Metab.,2002
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