Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy. uri icon

Overview

publication date

  • May 14, 2016

Research

keywords

  • Congenital Hyperinsulinism
  • Mosaicism
  • Mutation
  • Potassium Channels, Inwardly Rectifying
  • Uniparental Disomy

Identity

Scopus Document Identifier

  • 84967239661

Digital Object Identifier (DOI)

  • 10.1159/000446477

PubMed ID

  • 27174046

Additional Document Info

volume

  • 85

issue

  • 6