3-Hydroxy-3-methylglutaryl-CoA lyase deficiency studied using 2-dimensional proton nuclear magnetic resonance spectroscopy
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(86)81434-X/fullpdf
Reference10 articles.
1. The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria
2. 3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria
3. Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase
4. Dizygotic twins with 3-hydroxy-3-methylglutaric aciduria; unusual presentation, family studies and dietary management
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4. Inborn errors of metabolism associated with 3-methylglutaconic aciduria;Clinica Chimica Acta;2021-11
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