Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report
| Autor: | De Gier, C., Skacel, G., Walleczek, N.-K., Lischka, J., Baumgartner, M., Greber-Platzer, S. |
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| Zdroj: | In Atherosclerosis August 2022 355 |
| Databáze: | ScienceDirect |
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