Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene's candidacy in 6q16.1 deletions.
Am J Hum Genet
; 110(6): 998-1007, 2023 06 01.
Article
in En
| MEDLINE
| ID: mdl-37207645
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Prader-Willi Syndrome
/
Neurodevelopmental Disorders
/
Autism Spectrum Disorder
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Humans
Language:
En
Journal:
Am J Hum Genet
Year:
2023
Type:
Article
Affiliation country:
Germany