PLP1 mutations and central demyelination: Evidence from electrophysiologic phenotyping in female manifesting carriers. (2017)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1212/cpj.0000000000000346
PubMed Identifier: 29620084
Publication URI: http://europepmc.org/abstract/MED/29620084
Type: Journal Article/Review
Volume: 7
Parent Publication: Neurology. Clinical practice
Issue: 5
ISSN: 2163-0402