A de novo TOP2B variant associated with global developmental delay and autism spectrum disorder.
Mol Genet Genomic Med
; 8(3): e1145, 2020 03.
Article
in En
| MEDLINE
| ID: mdl-31953910
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Developmental Disabilities
/
DNA Topoisomerases, Type II
/
Autism Spectrum Disorder
/
Poly-ADP-Ribose Binding Proteins
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Child
/
Female
/
Humans
Language:
En
Journal:
Mol Genet Genomic Med
Year:
2020
Type:
Article
Affiliation country:
Japan