Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism
Author:
Funder
Else Kröner-Fresenius Stiftung
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference9 articles.
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4. Next-generation phenotyping using the parkin example: time to catch up with genetics;Grunewald;JAMA Neurol,2013
5. Genomic instability in the PARK2 locus is associated with Parkinson's disease;Ambroziak;J. Appl. Genet.,2015
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