📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

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