A coagulation defect arising from heterozygous premature termination of tissue factor.
J Clin Invest
; 130(10): 5302-5312, 2020 10 01.
Article
in En
| MEDLINE
| ID: mdl-32663190
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Thromboplastin
/
Frameshift Mutation
/
Blood Coagulation Disorders, Inherited
Type of study:
Prognostic_studies
Limits:
Animals
/
Female
/
Humans
/
Male
Language:
En
Journal:
J Clin Invest
Year:
2020
Type:
Article