Autosomal dominant GCH1 mutations causing spastic paraplegia at disease onset.
Parkinsonism Relat Disord
; 74: 12-15, 2020 05.
Article
in En
| MEDLINE
| ID: mdl-32278297
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Paraplegia
/
Parkinsonian Disorders
/
Dystonic Disorders
/
GTP Cyclohydrolase
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Adult
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Parkinsonism Relat Disord
Journal subject:
NEUROLOGIA
Year:
2020
Document type:
Article
Country of publication:
United kingdom