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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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Bibliografische gegevens
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1993
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC413260/
https://ncbi.nlm.nih.gov/pubmed/8382610
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