As part of an epidemiological study that aims to characterize chemically the mutation(s) in transthyretin (TTR) related to familial amyloidotic polyneuropathy (FAP) of different ethnic origins, studies were carried out on TTR from two FAP kindreds of Italian origin. Two different criteria were employed in the characterization of TTR from these kindreds: (1) immunoblotting of cyanogen bromide fragments for screening of TTR(Met30) and (2) isoelectric focusing. TTR(Met30) was not detected but other substitutions were demonstrated using isoelectric focusing techniques. One of the variants found is a basic TTR variant. The substitutions occurring in the variant TTRs of these two kindreds are not known and are presently under study
Background. Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) is a rare, progressive,...
The authors reviewed contribution of Kumamoto University group to the progress of the studies on tra...
Familial amyloid polyneuropathy (FAP) is an autosomal dominant disease characterized by deposition o...
We report the biochemical and molecular characterization of two new transthyretin (TTR) variants in ...
A Japanese family with atypical type I familial amyloidotic polyneuropathy (FAP) in Iiyama, Japan wa...
AbstractWe report the molecular analysis of the transthyretin gene in a large Italian pedigree with ...
Familial amyloid polyneuropathy (FAP) is a rare condition caused by mutations of the transthyretin (...
AbstractA novel variant transthyretin which contains a leucine-for-valine substitution at position 3...
A method is described for detecting carriers of a variant plasma prealbumin that is associated with ...
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...
A Dutch family with familial amyloidotic polyneuropathy associated with the transthyretin mutation V...
Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is caused by gain-of-toxic-function ...
Transthyretin-associated familial amyloid polyneuropathy (TTR-FAP) is an unusual but life-threatenin...
Mutations of the human transthyretin (TTR) gene have attracted medical interest as a cause of amyloi...
Background. Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) is a rare, progressive,...
The authors reviewed contribution of Kumamoto University group to the progress of the studies on tra...
Familial amyloid polyneuropathy (FAP) is an autosomal dominant disease characterized by deposition o...
We report the biochemical and molecular characterization of two new transthyretin (TTR) variants in ...
A Japanese family with atypical type I familial amyloidotic polyneuropathy (FAP) in Iiyama, Japan wa...
AbstractWe report the molecular analysis of the transthyretin gene in a large Italian pedigree with ...
Familial amyloid polyneuropathy (FAP) is a rare condition caused by mutations of the transthyretin (...
AbstractA novel variant transthyretin which contains a leucine-for-valine substitution at position 3...
A method is described for detecting carriers of a variant plasma prealbumin that is associated with ...
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...
A Dutch family with familial amyloidotic polyneuropathy associated with the transthyretin mutation V...
Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is caused by gain-of-toxic-function ...
Transthyretin-associated familial amyloid polyneuropathy (TTR-FAP) is an unusual but life-threatenin...
Mutations of the human transthyretin (TTR) gene have attracted medical interest as a cause of amyloi...
Background. Transthyretin-related familial amyloid polyneuropathy (ATTR-FAP) is a rare, progressive,...
The authors reviewed contribution of Kumamoto University group to the progress of the studies on tra...
Familial amyloid polyneuropathy (FAP) is an autosomal dominant disease characterized by deposition o...