Fibrinogen A α-chain amyloidosis associated with a rare frameshift pathogenic variant p.Arg547GlyfsTer21-Reference-Cited by-同舟云学术

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Fibrinogen A α-chain amyloidosis associated with a rare frameshift pathogenic variant p.Arg547GlyfsTer21

Published:2022-05-11 Issue:4 Volume:29 Page:276-277
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Tasaki Masayoshi¹²,Nomura Toshiya¹,Uchiyama Koichi³,Misumi Yohei¹,Nakahara Keiichi¹,Oyama Yuzo⁴,Uesugi Noriko⁴,Ueda Mitsuharu¹

Affiliation:

1. Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

2. Department of Biomedical Laboratory Sciences, Graduate School of Health Sciences, Kumamoto University, Kumamoto, Japan

3. Department of Urology, Konan Saint Hill Hospital, Ube, Japan

4. Department of Pathology, Fukuoka University School of Medicine, Fukuoka, Japan

Funder

Japanese Society of Laboratory Medicine Fund for the Promotion of Scientific Research

JSPS KAKENHI

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/13506129.2022.2074292

Reference5 articles.

1. Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics

2. VLITL is a major cross-β-sheet signal for fibrinogen Aα-chain frameshift variants

3. Typing of hereditary renal amyloidosis presenting with isolated glomerular amyloid deposition

4. Proteomic Analysis for the Diagnosis of Fibrinogen Aα-chain Amyloidosis

5. Fibrinogen alpha amyloidosis: insights from proteomics

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