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A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement. (2021)

First Author: Rebelo AP

Attributed to: The AAGGG repeat expansion in RFC1 associated with late-onset ataxia and sensory neuropathy: from genetic cause to defining the functional mechanism funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awab019

PubMed Identifier: 33889941

Publication URI: http://europepmc.org/abstract/MED/33889941

Type: Journal Article/Review

Volume: 144

Parent Publication: Brain : a journal of neurology

Issue: 4

ISSN: 0006-8950