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Molecular Genetics and Metabolism|November 14, 2000
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuriaK Tomoeda, H Awata, T Matsuura, et al.
Lancet (London, England)|July 13, 2002
How practical are recommendations for dietary control in phenylketonuria?J H Walter, F J White, S K Hall, et al.
Pediatric Research|March 3, 2001
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patientsL Bouchard, M F Robert, D Vinarov, et al.
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