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Volumn 270, Issue 2, 1998, Pages 195-201

Genetic variation in human serum albumin: A 313 Lys → Asn mutation in albumin reading identified by PCR analysis

Author keywords

Albumin Reading; Albumin variants; Bisalbuminaemia; PCR for mutant albumin gene

Indexed keywords

ALBUMIN;

EID: 0032559538     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-8981(97)00208-8     Document Type: Article
Times cited : (6)

References (16)
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    • Cloning of the Bacillus subtilis spoIIA and spoVA loci in phage ø0105DI:It
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    • Savva, D.1    Mandelstam, J.2
  • 9
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    • Screening of CNBr peptides from genetic variants of human serum albumin by isoelectric focusing
    • Peeters H, editor. Oxford: Pergamon Press
    • [9] Galliano M, Minchiotti L, Iadarola P, Porta F. Screening of CNBr peptides from genetic variants of human serum albumin by isoelectric focusing. In: Peeters H, editor. Protides of biological fluids. Oxford: Pergamon Press, 1986;34:815-8.
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    • Galliano, M.1    Minchiotti, L.2    Iadarola, P.3    Porta, F.4
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    • Two alloalbumins with identical electrophoretic mobility are produced by differently charged amino acid substitutions
    • [10] Minchiotti L, Galliano M, Stoppini M, Ferri G, Crespeau H, Rochu D, Porta F. Two alloalbumins with identical electrophoretic mobility are produced by differently charged amino acid substitutions. Biochim Biophys Acta 1992;1119:232-8.
    • (1992) Biochim Biophys Acta , vol.1119 , pp. 232-238
    • Minchiotti, L.1    Galliano, M.2    Stoppini, M.3    Ferri, G.4    Crespeau, H.5    Rochu, D.6    Porta, F.7
  • 11
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    • A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.