Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor
- PMID: 9041101
- DOI: 10.1056/NEJM199703063361005
Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical