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Volumn 27, Issue 2, 2007, Pages 88-90

Free functional muscle transfer failure and thrombophilic gene mutation as a potential risk factor: A case report

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5;

EID: 33947172574     PISSN: 07381085     EISSN: 10982752     Source Type: Journal    
DOI: 10.1002/micr.20312     Document Type: Article
Times cited : (11)

References (14)
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    • Heterozygosity for the factor V Leiden (G1691) mutation predisposes renal transplant recipients to thrombotic complications and graft loss
    • Wuthrich RP, Cicvara-Muzar S, Booy C, Maly FE. Heterozygosity for the factor V Leiden (G1691) mutation predisposes renal transplant recipients to thrombotic complications and graft loss. Transplantation 2005;72:549-550.
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    • Association of factor V Leiden mutation with delayed graft function, acute rejection episodes and long-term graft dysfunction in kidney transplant recipients
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  • 8
    • 0038489332 scopus 로고    scopus 로고
    • A FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers
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    • Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.