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Article

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

International journal of molecular sciences - 22 Jan 2018

Yazaki Masahide, Yoshinaga Tsuneaki, Sekijima Yoshiki, Kametani Fuyuki, Okumura Nobuo

Abstract excerpt

Hereditary fibrinogen Aα-chain amyloidosis (Aα-chain amyloidosis) is a type of autosomal dominant systemic amyloidosis caused by mutations in fibrinogen Aα-chain gene (FGA). Patients with Aα-chain amyloidosis have been mainly reported in Western countries but have been rarely reported in Asia, with only five patients with Aα-chain amyloidosis being reported in Korea, China, and Japan. Clinically, the most...

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Source

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Identifiers

PMID: 29361747
DOI: 10.3390/ijms19010320
PMCID: PMC5796263

Genes

FGA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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