Hereditary Hypofibrinogenemia with Hepatic Storage

Fibrinogen is a 340-kDa plasma glycoprotein constituted by two sets of symmetrical trimers, each formed by the Aα, Bβ, and γ chains (respectively coded by the FGA, FGB, and FGG genes). Quantitative fibrinogen deficiencies (hypofibrinogenemia, afibrinogenemia) are rare congenital disorders characteri...

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Detalles Bibliográficos
Autores principales: Asselta, Rosanna, Paraboschi, Elvezia Maria, Duga, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659954/
https://www.ncbi.nlm.nih.gov/pubmed/33105716
http://dx.doi.org/10.3390/ijms21217830

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659954/
https://www.ncbi.nlm.nih.gov/pubmed/33105716
http://dx.doi.org/10.3390/ijms21217830

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