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Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report (2024)

First Author: Imarisio A

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/10.1016/j.parkreldis.2024.106943

Publication URI: http://dx.doi.org/10.1016/j.parkreldis.2024.106943

Type: Journal Article/Review

Parent Publication: Parkinsonism & Related Disorders