Hyperinsulinism/hyperammonemia syndrome: insights into the regulatory role of glutamate dehydrogenase in ammonia metabolism
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference14 articles.
1. The hyperinsulinism-hyperammonemia syndrome: gain-of-function mutations of glutamate dehydrogenase;Stanley,2000
2. Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory GTP binding domain of glutamate dehydrogenase;MacMullen;J. Clin. Endocrinol. Metab.,2001
3. Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome;Hsu;J. Pediatr.,2001
4. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene;Stanley;N. Engl. J. Med.,1998
5. Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators;Stanley;Diabetes,2000
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