| Literature DB >> 8031680 |
Abstract
Significant advances were made this year in the understanding of serum amyloid A isotypes and in the definition of different amyloid light-chain proteins. Increasing numbers of hereditary amyloid-related transthyretin mutations have been reported (more than 30 to date). Two new hereditary amyloid proteins in several different kinships have appeared, ie, fibrinogen A alpha and lysozyme, each with a single point mutation. Both were found in patients with non-neurogenic hereditary amyloidosis with severe nephropathy. In islet amyloid polypeptide, the amyloid of adult-onset diabetes, the amino-acid sequence Ala-Ile-Leu-Ser at positions 25 to 28 appears to be critical for fibrillogenesis.Entities:
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Year: 1994 PMID: 8031680 DOI: 10.1097/00002281-199401000-00010
Source DB: PubMed Journal: Curr Opin Rheumatol ISSN: 1040-8711 Impact factor: 5.006