Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene's candidacy in 6q16.1 deletions. (2023)
Attributed to:
Rare Disease Research Platform: The renal ciliopathies national network (RCNN)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2023.04.010
PubMed Identifier: 37207645
Publication URI: http://europepmc.org/abstract/MED/37207645
Type: Journal Article/Review
Volume: 110
Parent Publication: American journal of human genetics
Issue: 6
ISSN: 0002-9297