Clinical Consequences and Molecular Bases of Low Fibrinogen Levels

The study of inherited fibrinogen disorders, characterized by extensive allelic heterogeneity, allows the association of defined mutations with specific defects providing significant insight into the location of functionally important sites in fibrinogen and fibrin. Since the identification of the f...

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Detalles Bibliográficos
Autores principales: Neerman-Arbez, Marguerite, Casini, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796141/
https://www.ncbi.nlm.nih.gov/pubmed/29316703
http://dx.doi.org/10.3390/ijms19010192

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796141/
https://www.ncbi.nlm.nih.gov/pubmed/29316703
http://dx.doi.org/10.3390/ijms19010192

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