Heterozygous ITGA2B Phe1024 Deletion Associated with Abnormal αIIbß3 Function in a Patient with Congenital Thrombocytopenia.
Semin Thromb Hemost
; 2024 Apr 11.
Article
in En
| MEDLINE
| ID: mdl-38604226
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Language:
En
Journal:
Semin Thromb Hemost
Year:
2024
Document type:
Article
Affiliation country:
China
Country of publication:
United States