Identification of two de novo variants causing inherited antithrombin deficiency by quantitative analysis of variant alleles.
Thromb Res
; 233: 37-40, 2024 01.
Article
in En
| MEDLINE
| ID: mdl-37995440
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Thrombophilia
/
Antithrombin III Deficiency
Limits:
Humans
Language:
En
Journal:
Thromb Res
Year:
2024
Type:
Article
Affiliation country:
Japan