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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...
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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5796141/ https://ncbi.nlm.nih.gov/pubmed/29316703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms19010192 |
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