Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs.

A Japanese family with atypical type I familial amyloidotic polyneuropathy (FAP) in Iiyama, Japan was studied. Most of the family members have dysfunctions in the central nervous system, in addition to typical symptoms of type I FAP. The transthyretin (TTR, also called prealbumin) gene of the atypic...

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Detalhes bibliográficos
Main Authors: Furuya, H, Yoshioka, K, Sasaki, H, Sakaki, Y, Nakazato, M, Matsuo, H, Nakadai, A, Ikeda, S, Yanagisawa, N
Formato: Artigo
Idioma:Inglês
Publicado em: 1987
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC442443/
https://ncbi.nlm.nih.gov/pubmed/3479441
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