A novel transthyretin mutation associated with familial amyloidotic polyneuropathy-Reference-Cited by-同舟云学术

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A novel transthyretin mutation associated with familial amyloidotic polyneuropathy

Published:1992-01 Issue:2 Volume:182 Page:520-526
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Murakami Tatsufumi,Maeda Shuichiro,Yi Shigehiro,Ikegawa Shinichi,Kawashima Eiji,Onodera Soukichi,Shimada Kazunori,Araki Shukuro

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference20 articles.

1. A PECULIAR FORM OF PERIPHERAL NEUROPATHY

2. Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)

3. Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

4. Identification of carriers of mutant prealbumin gene associated with familial amyloidotic polyneuropathy type I by Southern blot procedures: study of six pedigrees in the Arao district of Japan

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1. Transthyretin mutagenesis: impact on amyloidogenesis and disease;Critical Reviews in Clinical Laboratory Sciences;2024-06-07

2. Transthyretin as a target of alkylation and a potential biomarker for sulfur mustard poisoning: Electrophoretic and mass spectrometric identification and characterization;Drug Testing and Analysis;2021-08-24

3. Knee Arthrodesis in a Patient with Charcot Neuroarthropathy Secondary to Familial Amyloid Polyneuropathy;JBJS Case Connector;2017-12

4. Ocular Manifestations of Familial Transthyretin Amyloidosis;American Journal of Ophthalmology;2017-11

5. Extremely early onset hereditary ATTR amyloidosis with G47R (p.G67R) mutation;Amyloid;2016-05-20

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