Perry syndrome: Novel DCTN1 mutation in a large kindred and first observation of prodromal disease.
Parkinsonism Relat Disord
; 112: 105481, 2023 Jul.
Article
in En
| MEDLINE
| ID: mdl-37336025
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Parkinsonian Disorders
/
Depression
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Parkinsonism Relat Disord
Journal subject:
NEUROLOGIA
Year:
2023
Document type:
Article
Affiliation country:
Poland
Country of publication:
United kingdom