Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis

Proceedings of the National Academy of Sciences of the United States of America

Volumn 89, Issue 16, 1992, Pages 7389-7393

  Soutar, A K ^a   Hawkins, P N ^a   Vigushin, D M ^a   Tennent, G A ^a   Booth, S E ^a   Hutton, T ^a   Nguyen, O ^a   Totty, N F ^a   Feest, T G ^a   Hsuan, J J ^a   Pepys, M B ^a  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

Author keywords

mass spectrometry; protein sequencing

Indexed keywords

AMYLOID; APOLIPOPROTEIN A1; ARGININE; LEUCINE; POLYPEPTIDE;

ALLELE; AMINO ACID SUBSTITUTION; AMINO TERMINAL SEQUENCE; AMYLOIDOSIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; DNA DETERMINATION; GENE MUTATION; HUMAN; HUMAN TISSUE; HYBRIDIZATION; MASS SPECTROMETRY; MOLECULAR WEIGHT; PRIORITY JOURNAL;

EID: 0026712979     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.89.16.7389     Document Type: Article

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