Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders.
Brain
; 143(12): 3564-3573, 2020 12 01.
Article
in En
| MEDLINE
| ID: mdl-33242881
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Small-Conductance Calcium-Activated Potassium Channels
/
Neurodevelopmental Disorders
/
Movement Disorders
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Brain
Year:
2020
Type:
Article
Affiliation country:
France