Article
Phenotypic variability in a dystonia family with mutations in the manganese transporter gene.
Movement disorders : official journal of the Movement Disorder Society - 1 May 2013
Delnooz Cathérine C S, Wevers Ron A, Quadri Marialuisa, Clayton Peter T, Mills Philippa B, Tuschl Karin, Steenbergen Eric J, Bonifati Vincenzo, van de Warrenburg Bart P C
Abstract excerpt
No abstract is available from the source.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
