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
DOI10.3389/fneur.2018.00383

Authors from the University of Münster

Grauer, Oliver Martin
Department for Neurology
Meuth, Sven
Department for Neurology
Wiendl, Heinz Siegfried
Department for Neurology