Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference22 articles.
1. Glutaric aciduria type II: Report on a previously undescribed metabolic disorder;Przyrembel;Clin Chim Acta,1976
2. Glutaric aciduria type II;Sweetman;J Pediatr,1980
3. Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria: Possible inherited deficiency of an electron transfer flavoprotein;Goodman;Pediatr Res,1980
4. Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: Another possible case of glutaric aciduria type II;Gregersen;J Inher Metab Dis,1980
5. Neonatal glutaric aciduria type II: An X-linked recessive inherited disorder;Coudé;Hum Genet,1981
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4. Riboflavin (vitamin B2) and mitochondrial energy;Molecular Nutrition;2020
5. An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency;Molecular Genetics and Metabolism;2017-12
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