Cardiac amyloidosis associated with the transthyretin ile122 mutation in a caucasian family

Amyloid

Volumn 8, Issue 4, 2001, Pages 263-269

  Hamidi Asl, K ^a   Nakamura, M ^a   Yamashita, T ^a   Benson, M D ^a  

^a INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Amyloid; Cardiomyopathy; Genes; Heart failure; Transthyretin

Indexed keywords

ISOLEUCINE; PREALBUMIN;

AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CAUCASIAN; DIAGNOSTIC APPROACH ROUTE; DISEASE ASSOCIATION; DNA SEQUENCE; ETHNOLOGY; EXON; GENE MUTATION; HEART AMYLOIDOSIS; HUMAN; MALE; MORBIDITY; MORTALITY; NEGRO; PATHOPHYSIOLOGY; PEDIGREE; PRIORITY JOURNAL; PROTEIN VARIANT; RESTRICTIVE CARDIOMYOPATHY; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0035672528     PISSN: 13506129     EISSN: None     Source Type: Journal    
DOI: 10.3109/13506120108993823     Document Type: Article

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