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Volumn 31, Issue 3, 2014, Pages 226-230

Identification and genetic analysis of a factor IX gene intron 3 mutation in a hemophilia B pedigree in china;Çin'de bir hemofili b ailesinde faktör IX i̇ntron 3 mutasyonunun tani{dotless}mlamasi{dotless} ve genetik analizi

Author keywords

Factor ix; Hemophilia b; Intron 3; mRNA splice site; Mutation

Indexed keywords

BLOOD CLOTTING FACTOR 9;

EID: 84906683095     PISSN: 13007777     EISSN: 13085263     Source Type: Journal    
DOI: 10.4274/tjh.2013.0275     Document Type: Article
Times cited : (2)

References (8)
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    • Molecular pathology of haemophilia B in Turkish patients: Identification of a large deletion and 33 independent point mutations
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    • An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B
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    • Rallapalli, P.M.1    Kemball-Cook, G.2    Tuddenham, E.G.3    Gomez, K.4    Perkins, S.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.