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A rare cause of autosomal recessive ataxia with very late diagnosis and prolonged disease course. (2024)

First Author: Bhattacharjee S

Attributed to: Pleiotropic disorders of mitochondrial translation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00415-024-12778-3

PubMed Identifier: 39666069

Publication URI: http://europepmc.org/abstract/MED/39666069

Type: Journal Article/Review

Volume: 272

Parent Publication: Journal of neurology

Issue: 1

ISSN: 0340-5354