Are some C19orf12 variants monoallelic for neurological disorders? (2019)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.parkreldis.2019.05.020
PubMed Identifier: 31105013
Publication URI: http://europepmc.org/abstract/MED/31105013
Type: Journal Article/Review
Volume: 65
Parent Publication: Parkinsonism & related disorders
ISSN: 1353-8020