De novo variants in ATP2B1 lead to neurodevelopmental delay.
Am J Hum Genet
; 109(5): 944-952, 2022 05 05.
Article
in En
| MEDLINE
| ID: mdl-35358416
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Neurodevelopmental Disorders
/
Intellectual Disability
/
Nervous System Malformations
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Am J Hum Genet
Year:
2022
Document type:
Article