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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2018
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| 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 |