ℹ️
🇬🇧
Search
Search for people relevant for "Snf2h"
Snf2h
Person
Class
Person
Publication
Programmes
Gisela Slaats
Person without affiliation with CUNI
1 publication
Publication
publication
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
2023 |
First Faculty of Medicine, Second Faculty of Medicine
Loading network view...