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