Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two sicilian kindreds with hereditary amyloidosis-Reference-Cited by-同舟云学术

Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two sicilian kindreds with hereditary amyloidosis

Published:1992 Issue:3 Volume:1 Page:211-215
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Almeida Maria do Rosário,Ferlini Alessandra,Forabosco Antonino,Gawinowicz Maryann,Costa Pedro P.,Salvi Fabrizio,Plasmati Rosaria,Tassinari Carlo A.,Altland Klaus,Saraiva Maria Joã

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. Prenatal diagnosis of familial amyloidotic polyneuropathy: evidence for an early expression of the associated transthyretin methionine 30

2. Characterization of a basic transthyretin variant - TTR Arg 102 - in the German population

3. Paraffin oil protected high resolution hybrid isoelectric focusing for the demonstration of substitutions of neutral amino acids in denatured proteins: The case of four human transthyretin (prealbumin) variants associated with familial amyloidotic polyneuropathy

4. Structure of prealbumin: Secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 Å

5. Evidence that the amyloid fibril protein in senile systemic amyloidosis is derived from normal prealbumin

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