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

Hum Mutat. 2017 Oct;38(10):1442-1444. doi: 10.1002/humu.23289. Epub 2017 Aug 1.
No abstract available

Keywords: UCP2; congenital hyperinsulinism; genetics; hypoglycaemia.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cohort Studies
  • Congenital Hyperinsulinism / genetics*
  • Databases, Genetic
  • Genetic Predisposition to Disease
  • Humans
  • Infant, Newborn
  • Mutation*
  • Sequence Analysis, DNA / methods*
  • Uncoupling Protein 2 / genetics*

Substances

  • UCP2 protein, human
  • Uncoupling Protein 2