Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.
Eur J Hum Genet
; 28(4): 532, 2020 Apr.
Article
in En
| MEDLINE
| ID: mdl-31506600
Full text:
1
Database:
MEDLINE
Type of study:
Risk_factors_studies
Language:
En
Year:
2020
Type:
Article