Identification of a Rare Novel KMT2C Mutation That Presents with Schizophrenia in a Multiplex Family.
J Pers Med
; 11(12)2021 Nov 25.
Article
in En
| MEDLINE
| ID: mdl-34945726
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Diagnostic_studies
/
Prognostic_studies
Language:
En
Journal:
J Pers Med
Year:
2021
Document type:
Article
Affiliation country:
Taiwan
Country of publication:
Switzerland