A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Am J Hum Genet
; 111(6): 1239, 2024 Jun 06.
Article
in En
| MEDLINE
| ID: mdl-38723631
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Language:
En
Journal:
Am J Hum Genet
Year:
2024
Type:
Article