Transthyretin mutations in health and disease

Human Mutation

Volumn 5, Issue 3, 1995, Pages 191-196

  João, Maria ^a,b   Saraiva, Mascarenhas ^a,b  

^a UNIVERSITY OF PORTO   (Portugal)

^b Centro de Estudos de Paramiloidose   (Portugal)

Author keywords

Familial amyloid cardiomyopathy; Familial amyloid polyneuropathy; Hyperthyroxinemia; Transthyretin

Indexed keywords

AMYLOID; PREALBUMIN; RETINOL BINDING PROTEIN; THYROXINE;

AMYLOID NEUROPATHY; AMYLOIDOSIS; ARTICLE; CARDIOMYOPATHY; GENE MUTATION; GENETIC HETEROGENEITY; HEART AMYLOIDOSIS; HUMAN; HYPERTHYROXINEMIA; NEUROPATHY; NONHUMAN; PRIORITY JOURNAL; THYROID FUNCTION; VITREOUS OPACITY;

ALLELES; AMYLOIDOSIS; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; GENE FREQUENCY; GENETIC HETEROGENEITY; HUMAN; MALE; MUTATION; PREALBUMIN; PROTEIN STRUCTURE, TERTIARY;

EID: 0028969996     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1380050302     Document Type: Article

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