A low amyloidogenic E61K transthyretin mutation may cause familial amyloid polyneuropathy-Reference-Cited by-同舟云学术

A low amyloidogenic E61K transthyretin mutation may cause familial amyloid polyneuropathy

Published:2020-09-20 Issue:6 Volume:156 Page:957-966
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Murakami Tatsufumi¹^ORCID,Yokoyama Takeshi²,Mizuguchi Mineyuki²,Toné Shigenobu³,Takaku Shizuka⁴,Sango Kazunori⁴^ORCID,Nishimura Hirotake⁵,Watabe Kazuhiko⁶,Sunada Yoshihide¹

Affiliation:

1. Department of Neurology Kawasaki Medical School Kurashiki Japan

2. Faculty of Pharmaceutical Sciences University of Toyama Toyama Japan

3. Graduate School of Science and Engineering Tokyo Denki University Hatoyama Saitama Japan

4. Diabetic Neuropathy Project Department of Diseases and Infection Tokyo Metropolitan Institute of Medical Science Tokyo Japan

5. Department of Pathology Kawasaki Medical School Kurashiki Japan

6. Department of Medical Technology Faculty of Health Sciences Kyorin University Tokyo Japan

Funder

Kawasaki Medical School

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jnc.15162

Reference48 articles.

1. First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy

2. PHENIX: a comprehensive Python-based system for macromolecular structure solution

3. Only amyloidogenic intermediates of transthyretin induce apoptosis

4. A PECULIAR FORM OF PERIPHERAL NEUROPATHY

5. Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients

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