A Novel PKD1 Mutation Associated With Autosomal Dominant Kidney Disease and Cerebral Cavernous Malformation

Thomas C, Zuehlsdorf A, Hoertnagel K, Mulahasanovic L, Grauer OM, Kuempers P, Wiendl H, Meuth SG

Research article (journal) | Peer reviewed

Details about the publication

JournalFrontiers in Neurology
Volume9
StatusPublished
Release year2018
Language in which the publication is writtenEnglish

Authors from the University of Münster

Grauer, Oliver Martin
Meuth, Sven
Wiendl, Heinz Siegfried