Correspondence on "Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype" by Zanoni et al.
Genet Med
; 24(3): 754-756, 2022 03.
Article
in En
| MEDLINE
| ID: mdl-34906509
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Wolf-Hirschhorn Syndrome
Type of study:
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Genet Med
Journal subject:
GENETICA MEDICA
Year:
2022
Type:
Article