Inborn errors of metabolism associated with 3-methylglutaconic aciduria
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference82 articles.
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3. A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency;Santarelli;Ital. J. Pediatr.,2013
4. Leucine Loading Test is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH Defect;Wortmann;JIMD Rep.,2014
5. X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria;Kelley;J. Pediatr.,1991
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