A novel PCDH19 mutation inherited from an unaffected mother.
Pediatr Neurol
; 46(6): 397-400, 2012 Jun.
Article
in En
| MEDLINE
| ID: mdl-22633638
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Cadherins
/
Epilepsy
/
Heterozygote
/
Mothers
/
Mutation
Limits:
Adolescent
/
Female
/
Humans
Language:
En
Journal:
Pediatr Neurol
Journal subject:
NEUROLOGIA
/
PEDIATRIA
Year:
2012
Type:
Article
Affiliation country:
Bulgaria