Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders.
Am J Med Genet A
; 188(9): 2750-2759, 2022 09.
Article
in En
| MEDLINE
| ID: mdl-35543142
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Retinitis Pigmentosa
/
Neurodevelopmental Disorders
/
Autism Spectrum Disorder
Type of study:
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Am J Med Genet A
Year:
2022
Document type:
Article