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Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease
C E Mize1, L J Waber, T Anderson
1University of Texas Southwestern Medical Center, Department of Pediatrics, Dallas 75235-9063, USA.
Journal of Inherited Metabolic Disease
|July 1, 1997
Abstract
No abstract available in PubMed .
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