Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy.
Overview
publication date
- May 14, 2016
published in
- Hormone research in paediatrics Journal
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
has global citation frequency
volume
- 85
issue
- 6