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

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...

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Detalles Bibliográficos
Autores principales: Yazaki, Masahide, Yoshinaga, Tsuneaki, Sekijima, Yoshiki, Kametani, Fuyuki, Okumura, Nobuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796263/
https://www.ncbi.nlm.nih.gov/pubmed/29361747
http://dx.doi.org/10.3390/ijms19010320

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796263/
https://www.ncbi.nlm.nih.gov/pubmed/29361747
http://dx.doi.org/10.3390/ijms19010320

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