Structure of Met30 variant of transthyretin and its amyloidogenic implications.

Familial amyloidotic polyneuropathy (FAP) is an autosomal dominant hereditary type of lethal amyloidosis involving single (or double) amino acid substitutions in the amyloidogenic protein transthyretin (TTR). The most common type of FAP (Type I, or Portuguese) is characterized by a Val-->Met subs...

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Detalhes bibliográficos
Main Authors: Terry, C J, Damas, A M, Oliveira, P, Saraiva, M J, Alves, I L, Costa, P P, Matias, P M, Sakaki, Y, Blake, C C
Formato: Artigo
Idioma:Inglês
Publicado em: 1993
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC413260/
https://ncbi.nlm.nih.gov/pubmed/8382610
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