Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy.
Eur J Hum Genet
; 31(3): 345-352, 2023 03.
Article
in En
| MEDLINE
| ID: mdl-36564538
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Autistic Disorder
/
Epilepsy
/
Neurodevelopmental Disorders
/
Intellectual Disability
Limits:
Humans
Language:
En
Journal:
Eur J Hum Genet
Year:
2023
Document type:
Article