Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia. uri icon

Overview

publication date

  • August 1, 2017

Research

keywords

  • Congenital Hyperinsulinism
  • Mutation
  • Sequence Analysis, DNA
  • Uncoupling Protein 2

Identity

PubMed Central ID

  • PMC6815675

Scopus Document Identifier

  • 85026533685

Digital Object Identifier (DOI)

  • 10.1002/humu.23289

PubMed ID

  • 28681398

Additional Document Info

volume

  • 38

issue

  • 10