3-Methylcrotonylglycine excretion in 3-hydroxy-3-methylglutaric aciduria
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference16 articles.
1. 3-Hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria
2. The urinary organic acid profile associated with 3-hydroxy-3-methylglutaric aciduria
3. $beta;-HYDROXYISOVALERIC ACIDURIA AND $beta;-METHYLCROTONYLGLYCINURIA: A NEW INBORN ERROR OF METABOLISM
4. BIOTIN-RESPONSIVE β-METHYLCROTONYLGLYCINURIA
5. Identification of N-acylglycines by gas-liquid chromatography
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1. Molecular genetics of HMG-CoA lyase deficiency;Molecular Genetics and Metabolism;2007-11
2. Molecular basis of 3-hydroxy-3-methylglutaric aciduria;Journal of Physiology and Biochemistry;2003-12
3. Mass spectrometry in disorders of organic acid metabolism;Clinica Chimica Acta;1995-10
4. 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients;European Journal of Pediatrics;1988-12
5. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: A review;Journal of Inherited Metabolic Disease;1986-09
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