Fibrinogen A α-chain amyloidosis associated with a rare frameshift pathogenic variant p.Arg547GlyfsTer21
Amyloid
.
2022 Dec;29(4):276-277.
doi: 10.1080/13506129.2022.2074292.
Epub 2022 May 11.
Authors
Masayoshi Tasaki
1
2
,
Toshiya Nomura
1
,
Koichi Uchiyama
3
,
Yohei Misumi
1
,
Keiichi Nakahara
1
,
Yuzo Oyama
4
,
Noriko Uesugi
4
,
Mitsuharu Ueda
1
Affiliations
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.
PMID:
35543193
DOI:
10.1080/13506129.2022.2074292
No abstract available
Publication types
Letter
MeSH terms
Amyloidosis* / genetics
Amyloidosis* / pathology
Fibrinogen* / genetics
Frameshift Mutation / genetics
Humans
Substances
Fibrinogen