FGB mutations leading to congenital quantitative fibrinogen deficiencies: An update and report of four novel mutations
| Autor: | Casini, A., Lukowski, S., Quintard, V. Louvain, Crutu, A., Zak, M., Regazzoni, S., de Moerloose, P., Neerman-Arbez, M. |
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| Zdroj: | In Thrombosis Research May 2014 133(5):868-874 |
| Databáze: | ScienceDirect |
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