Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.
Transl Psychiatry
; 7(8): e1184, 2017 08 01.
Article
in En
| MEDLINE
| ID: mdl-28763059
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Schizophrenia
/
Autism Spectrum Disorder
/
CX3C Chemokine Receptor 1
Type of study:
Etiology_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Adult
/
Aged
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Transl Psychiatry
Year:
2017
Document type:
Article