Variants in the new E1' cryptic exon of the VHL gene associated with congenital erythrocytosis-Description of three cases.
EJHaem
; 3(3): 989-991, 2022 Aug.
Article
in En
| MEDLINE
| ID: mdl-36051068
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Risk_factors_studies
Language:
En
Journal:
EJHaem
Year:
2022
Type:
Article