DCTN1 mutation associated parkinsonism: case series of three new families with perry syndrome. (2022)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00415-022-11308-3

PubMed Identifier: 35895135

Publication URI: http://europepmc.org/abstract/MED/35895135

Type: Journal Article/Review

Volume: 269

Parent Publication: Journal of neurology

Issue: 12

ISSN: 0340-5354