Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism. (2022)
Attributed to:
The University of Manchester (UoM) bid for phase 7 of MRC Confidence in Concept (CiC) funding
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41588-022-01204-x
PubMed Identifier: 36333503
Publication URI: http://europepmc.org/abstract/MED/36333503
Type: Journal Article/Review
Volume: 54
Parent Publication: Nature genetics
Issue: 11
ISSN: 1061-4036