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Volumn 36, Issue 2, 2006, Pages 265-268

Novel and Mediterranean β thalassemia mutations in the indigenous Northern Ireland population

Author keywords

thalassemia; thalassemia trait; +IVS I 110 (G A); 039 (C T); 0IVS II 850 (G A)

Indexed keywords

BETA GLOBIN;

EID: 33645275494     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2005.12.005     Document Type: Article
Times cited : (14)

References (17)
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    • Orkin, S.H.1    Kazazian, H.H.2    Antonarakis, S.E.3    Goff, S.C.4    Boehm, C.D.5    Sexton, J.P.6    Waber, P.G.7    Giardina, P.J.V.8
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    • History and origin of β-thalassaemia in Turkey: Sequence haplotype diversity of β-globin genes
    • G.O. Tadmouri, N. Garguier, J. Demont, P. Perrin, and A.N. Başak History and origin of β-thalassaemia in Turkey: sequence haplotype diversity of β-globin genes Hum. Biol. 73 2001 661 674
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    • Zahed, L.1    Demont, J.2    Bouhass, R.3    Trabuchet, G.4    Hänni, C.5    Zalloua, P.6    Perrin, P.7
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    • A mutation of the β-globin gene initiation codon, ATG → AAG, found in a French Caucasian man
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    • H.H. Kazazian Jr., C.E. Dowling, R.L. Hurwitz, M. Coleman, and J.G. Adams III Thalassaemia mutations in exon 3 of the β-globin gene often cause a dominant form of thalassemia and show no predilection for malarial-endemic regions of the world Am. J. Hum. Gen. 45 1989 A242
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.