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.
