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PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease. (2018)

First Author: Juneja M

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/10.1136/jnnp-2017-317562

PubMed Identifier: 29449460

Publication URI: http://europepmc.org/abstract/MED/29449460

Type: Journal Article/Review

Volume: 89

Parent Publication: Journal of neurology, neurosurgery, and psychiatry

Issue: 8

ISSN: 0022-3050