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Volumn 104, Issue 2, 2013, Pages 159-165

The ABCB6 mutation p.Arg192Trp is a recessive mutation causing the Lan- blood type

Author keywords

ABCB6; Lan blood group antigen; Missense mutation; Null allele

Indexed keywords

ABC TRANSPORTER; ABCB6 PROTEIN; BLOOD GROUP ANTIGEN; LAN BLOOD GROUP ANTIGEN; UNCLASSIFIED DRUG;

EID: 84872612739     PISSN: 00429007     EISSN: 14230410     Source Type: Journal    
DOI: 10.1111/j.1423-0410.2012.01650.x     Document Type: Article
Times cited : (17)

References (7)
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  • 2
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    • Hemolytic disease of the newborn due to anti-Lan
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  • 3
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  • 4
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    • ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis
    • Helias V, Saison C, Ballif BA, et al. : ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis. Nat Genet 2012; 44:170-173
    • (2012) Nat Genet , vol.44 , pp. 170-173
    • Helias, V.1    Saison, C.2    Ballif, B.A.3
  • 5
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    • SIFT: predicting amino acid changes that affect protein function
    • Ng PC, Henikoff S: SIFT: predicting amino acid changes that affect protein function. Nucleic Acids Res 2003; 31:3812-3814
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    • Ng, P.C.1    Henikoff, S.2
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    • Prediction of deleterious human alleles
    • Sunyaev S, Ramensky V, Koch I, et al. : Prediction of deleterious human alleles. Hum Mol Genet 2001; 10:591-597
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  • 7
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    • Targeted degradation of ABC transporters in health and disease
    • Nikles D, Tampe R: Targeted degradation of ABC transporters in health and disease. J Bioenerg Biomembr 2007; 39:489-497
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    • Nikles, D.1    Tampe, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.