Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis. (2016)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.neurobiolaging.2016.07.024
PubMed Identifier: 27594680
Publication URI: http://europepmc.org/abstract/MED/27594680
Type: Journal Article/Review
Volume: 47
Parent Publication: Neurobiology of aging
ISSN: 0197-4580