Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia. (2017)
Attributed to:
Identifying non-coding mutations in early-onset diabetes
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.23289
PubMed Identifier: 28681398
Publication URI: http://europepmc.org/abstract/MED/28681398
Type: Journal Article/Review
Volume: 38
Parent Publication: Human mutation
Issue: 10
ISSN: 1059-7794