Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia.
J Hum Genet
; 64(8): 803-813, 2019 Aug.
Article
in En
| MEDLINE
| ID: mdl-31165786
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenotype
/
Histone-Lysine N-Methyltransferase
/
Genetic Predisposition to Disease
/
Dystonia
/
Genetic Association Studies
/
Mutation
Type of study:
Prognostic_studies
Limits:
Child
/
Child, preschool
/
Female
/
Humans
/
Male
Language:
En
Journal:
J Hum Genet
Journal subject:
GENETICA MEDICA
Year:
2019
Type:
Article
Affiliation country:
Germany