Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders

Congenital fibrinogen disorders can be quantitative (afibrinogenemia, hypofibrinogenemia) or functional (dysfibrinognemia). To date, several genetic variants have been identified in individuals with fibrinogen disorders. The complexity of the fibrinogen molecules, formed by three non-identical chain...

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Detalles Bibliográficos
Autores principales: Tiscia, Giovanni Luca, Margaglione, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032319/
https://www.ncbi.nlm.nih.gov/pubmed/29844251
http://dx.doi.org/10.3390/ijms19061597

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032319/
https://www.ncbi.nlm.nih.gov/pubmed/29844251
http://dx.doi.org/10.3390/ijms19061597

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