Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations.
Haematologica
; 107(10): 2511-2516, 2022 10 01.
Article
in En
| MEDLINE
| ID: mdl-35796010
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Blood Platelet Disorders
/
Core Binding Factor Alpha 2 Subunit
Type of study:
Diagnostic_studies
Limits:
Child
/
Humans
Language:
En
Journal:
Haematologica
Year:
2022
Type:
Article