The prothrombin 20210 A allele is frequently coinherited in young carriers of the factor V Arg 506 to Gln mutation with venous thrombophilia

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Bibliographic Details
Published inBlood Vol. 91; no. 6; pp. 2209 - 2210
Main Authors Ehrenforth, S, Ludwig, G, Klinke, S, Krause, M, Scharrer, I, Nowak-Gottl, U
Format Journal Article
LanguageEnglish
Published United States 15.03.1998
Subjects
Adolescent
Adult
Age of Onset
Alleles
Comorbidity
Factor V - genetics
Female
Gene Frequency
Germany - epidemiology
Humans
Male
Middle Aged
Prothrombin - analysis
Prothrombin - genetics
Risk Factors
Thrombophilia - epidemiology
Thrombophilia - genetics
Germany
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Bibliography:SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.V91.6.2209