AbstractWe report the molecular analysis of the transthyretin gene in a large Italian pedigree with familial amyloidotic polyneuropathy and demonstrate the presence of a Met30 mutation. The usefulness of the genetic analysis in the identification of presymptomatic persons and the diagnosis of individuals with partial symptoms is discussed
PubMed ID: 27238058Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is an autosomal d...
© 2016 The Authors Muscle & Nerve Published by Wiley Periodicals, Inc. This is an open access articl...
The authors reviewed contribution of Kumamoto University group to the progress of the studies on tra...
AbstractWe report the molecular analysis of the transthyretin gene in a large Italian pedigree with ...
PubMedID: 2174830A Turkish family is described with two members suffering from familial amyloidotic ...
As part of an epidemiological study that aims to characterize chemically the mutation(s) in transthy...
金沢大学がん研究所がん分子細胞制御A Japanese family with atypical type I familial amyloidotic polyneuropathy (FAP) in...
A Japanese family with atypical type I familial amyloidotic polyneuropathy (FAP) in Iiyama, Japan wa...
Introduction: Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) typically arises as an...
Familial amyloidotic polyneuropathy type 1 (FAP1, MIM176300) is an autosomal dominant disease caused...
We report on the genetic and molecular characterisation of an Italian family with a late-onset, auto...
International audienceObjective To compare the natural history of familial transthyretin amyloid pol...
Familial amyloid polyneuropathy (FAP) is a progressive systemic autosomal dominant disease caused by...
Familial amyloid polyneuropathy (FAP) is a progressive systemic autosomal dominant disease caused by...
Familial amyloid polyneuropathy (FAP) is a rare condition caused by mutations of the transthyretin (...
PubMed ID: 27238058Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is an autosomal d...
© 2016 The Authors Muscle & Nerve Published by Wiley Periodicals, Inc. This is an open access articl...
The authors reviewed contribution of Kumamoto University group to the progress of the studies on tra...
AbstractWe report the molecular analysis of the transthyretin gene in a large Italian pedigree with ...
PubMedID: 2174830A Turkish family is described with two members suffering from familial amyloidotic ...
As part of an epidemiological study that aims to characterize chemically the mutation(s) in transthy...
金沢大学がん研究所がん分子細胞制御A Japanese family with atypical type I familial amyloidotic polyneuropathy (FAP) in...
A Japanese family with atypical type I familial amyloidotic polyneuropathy (FAP) in Iiyama, Japan wa...
Introduction: Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) typically arises as an...
Familial amyloidotic polyneuropathy type 1 (FAP1, MIM176300) is an autosomal dominant disease caused...
We report on the genetic and molecular characterisation of an Italian family with a late-onset, auto...
International audienceObjective To compare the natural history of familial transthyretin amyloid pol...
Familial amyloid polyneuropathy (FAP) is a progressive systemic autosomal dominant disease caused by...
Familial amyloid polyneuropathy (FAP) is a progressive systemic autosomal dominant disease caused by...
Familial amyloid polyneuropathy (FAP) is a rare condition caused by mutations of the transthyretin (...
PubMed ID: 27238058Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is an autosomal d...
© 2016 The Authors Muscle & Nerve Published by Wiley Periodicals, Inc. This is an open access articl...
The authors reviewed contribution of Kumamoto University group to the progress of the studies on tra...