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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, C. A., Fang, J., Kutyna, K., Hsu, B. Y., Ming, J. E., Glaser, B., Poncz, M.Volume:
49
Language:
english
Journal:
Diabetes
DOI:
10.2337/diabetes.49.4.667
Date:
April, 2000
File:
PDF, 169 KB
english, 2000