Familial chylomicronemia syndrome
"Familial chylomicronemia syndrome (FCS) is an ultra-rare genetic disorder characterized by the abnormal build-up of chylomicrons, the largest type of lipoprotein, which transport dietary fat from the gut to the rest of the body. Patients with FCS often experience severe symptoms, the most fear...
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| Format: | Elektronisch E-Book |
| Sprache: | English |
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Abingdon, Oxford
Karger
2022
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| Schriftenreihe: | Fast facts
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