CORRIGENDUM FOR “Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2”

Gelijkaardige items

• Novel Hypoglycemia Phenotype in Congenital Hyperinsulinism Due to Dominant Mutations of Uncoupling Protein 2
  door: Ferrara, Christine T., et al.
  Gepubliceerd in: (2016)
• Novel dominant K(ATP) channel mutations in infants with congenital hyperinsulinism: Validation by in vitro expression studies and in vivo carrier phenotyping
  door: Boodhansingh, Kara E., et al.
  Gepubliceerd in: (2019)
• Congenital hyperinsulinism due to NEUROD1 gene mutation
  door: In Kim, et al.
  Gepubliceerd in: (2025-10-01)
• Congenital intrahepatic portocaval shunts and hypoglycemia due to secondary hyperinsulinism: a case report and review of the literature
  door: Weigert, Alexander, et al.
  Gepubliceerd in: (2018)
• Novel Presentations of Congenital Hyperinsulinism due to Mutations in the MODY genes: HNF1A and HNF4A
  door: Stanescu, Diana E., et al.
  Gepubliceerd in: (2012)