Kidney International Reports (Oct 2020)
Polycystic Kidney Disease Caused by Bilineal Inheritance of Truncating PKD1 as Well as PKD2 Mutations
- Monique Losekoot,
- Esther Meijer,
- E. Christiaan Hagen,
- Vladimir Belostotsky,
- Martin de Borst,
- Aart Tholens,
- Marion Phylipsen,
- York Pei,
- Ron T. Gansevoort,
- Dorien J.M. Peters
Affiliations
- Monique Losekoot
- Department of Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands
- Esther Meijer
- Department of Nephrology, University Medical Center Groningen, University Hospital Groningen, Groningen, Netherlands
- E. Christiaan Hagen
- Department of Internal Medicine, Meander Medisch Centrum, Amersfoort, Netherlands
- Vladimir Belostotsky
- Department of Pediatrics, Faculty of Health Sciences, McMaster Children’s Hospital, Hamilton, Ontario, Canada
- Martin de Borst
- Department of Nephrology, University Medical Center Groningen, University Hospital Groningen, Groningen, Netherlands
- Aart Tholens
- Department of Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands
- Marion Phylipsen
- Department of Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands
- York Pei
- Division of Nephrology, University Health Network, University of Toronto, Toronto, Ontario, Canada
- Ron T. Gansevoort
- Department of Nephrology, University Medical Center Groningen, University Hospital Groningen, Groningen, Netherlands
- Dorien J.M. Peters
- Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands; Correspondence: Dorien J.M. Peters, Department of Human Genetics, Postzone S-04-P, Leiden University Medical Center (LUMC), P.O. Box 9600, 2300 RC Leiden, Netherlands.
- Journal volume & issue
-
Vol. 5,
no. 10
pp. 1828 – 1832
