Hereditary systemic amyloidosis associated with a new apolipoprotein AII stop codon mutation Stop78Arg

Kidney International

Volumn 64, Issue 1, 2003, Pages 11-16

  Yazaki, Masahide ^b   Liepnieks, Juris J ^b   Barats, Mark S ^b   Cohen, Arthur H ^b   Benson, Merrill D ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

Amyloidosis; Apolipoprotein AII; Cardiomyopathy; Nephropathy; Peptide elongation; Stop codon mutations

Indexed keywords

AMYLOID PROTEIN; APOLIPOPROTEIN; APOLIPOPROTEIN A2; ARGININE; DNA; PYROPHOSPHATE TECHNETIUM TC 99M;

ADULT; AMYLOIDOSIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CODON; DNA SEQUENCE; GENETIC DISORDER; HEART MUSCLE; HEART SCINTISCANNING; HUMAN; HUMAN TISSUE; IMMUNOBLOTTING; KIDNEY AMYLOIDOSIS; KIDNEY BIOPSY; KIDNEY DISEASE; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0037792997     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2003.00047.x     Document Type: Article

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