Detection and Gene Mutation Analysis of Three Variations in Two Unrelated Chinese Hereditary Coagulation Factor XI Deficiency Families.
Acta Haematol
; 145(6): 611-618, 2022.
Article
in En
| MEDLINE
| ID: mdl-35850092
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Factor XI
/
Factor XI Deficiency
Type of study:
Diagnostic_studies
Limits:
Humans
Language:
En
Journal:
Acta Haematol
Year:
2022
Type:
Article
Affiliation country:
China