The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype. (2014)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s00401-014-1251-9
PubMed Identifier: 24493408
Publication URI: http://europepmc.org/abstract/MED/24493408
Type: Journal Article/Review
Volume: 127
Parent Publication: Acta neuropathologica
Issue: 3
ISSN: 0001-6322