Congenital hyperinsulinism: marked clinical heterogeneity in siblings with identical mutations in the ABCC8 gene. Article uri icon

Overview

publication date

  • February 1, 2012

Research

keywords

  • ATP-Binding Cassette Transporters
  • Congenital Hyperinsulinism
  • Mutation
  • Potassium Channels, Inwardly Rectifying
  • Receptors, Drug

Identity

Scopus Document Identifier

  • 84855465223

Digital Object Identifier (DOI)

  • 10.1111/j.1365-2265.2011.04203.x

PubMed ID

  • 21851374

Additional Document Info

volume

  • 76

issue

  • 2