De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement.
Am J Hum Genet
; 109(10): 1932-1943, 2022 10 06.
Article
in En
| MEDLINE
| ID: mdl-36206744
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Intellectual Disability
Type of study:
Risk_factors_studies
Limits:
Animals
/
Humans
Language:
En
Journal:
Am J Hum Genet
Year:
2022
Type:
Article
Affiliation country:
United States