Molecular and genetic analysis of a compound heterozygote for dysprothrombinemia of prothrombin Tokushima and hypoprothrombinemia.
Am J Hum Genet
; 51(6): 1386-95, 1992 Dec.
Article
in En
| MEDLINE
| ID: mdl-1334372
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Blood Coagulation Disorders
/
Prothrombin
/
Genetic Carrier Screening
/
Hypoprothrombinemias
Limits:
Child
/
Female
/
Humans
/
Male
Language:
En
Journal:
Am J Hum Genet
Year:
1992
Document type:
Article
Affiliation country:
Japan
Country of publication:
United States