Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease (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.kint.2023.07.021
PubMed Identifier: 37598857
Publication URI: http://europepmc.org/abstract/MED/37598857
Type: Journal Article/Review
Parent Publication: Kidney International
Issue: 5