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
Volume: 104
Parent Publication: Kidney international
Issue: 5
ISSN: 0085-2538