Expanding the Phenotype of Dystonia-Deafness Syndrome Caused by
ACTB
Gene Mutation
Mov Disord Clin Pract
.
2019 Nov 14;7(1):86-87.
doi: 10.1002/mdc3.12854.
eCollection 2020 Jan.
Authors
Julian Letícia Freitas
1
,
Thiago Cardoso Vale
2
,
Orlando G P Barsottini
1
,
José Luiz Pedroso
1
Affiliations
1
Division of General Neurology and Ataxia Unit, Department of Neurology Universidade Federal de São Paulo São Paulo Brazil.
2
Movement Disorders Unit, Service of Neurology University Hospital, Universidade Federal de Juiz de Fora Juiz de Fora Brazil.
PMID:
31970217
PMCID:
PMC6962673
DOI:
10.1002/mdc3.12854
No abstract available
Publication types
Case Reports