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Pediatric Research|August 29, 2000
Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotypeB W Weston, J L Lin, J Muenzer, et al.
Pediatric Research|January 3, 2001
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiencyM J Corydon, J Vockley, P Rinaldo, et al.
Pediatrics|April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patientsK M Gibson, E Christensen, C Jakobs, et al.
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