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Dissection of Clinical and Gene Expression Signatures of Familial versus Multifactorial Chylomicronemia
Familial chylomicronemia syndrome (FCS) is a rare disorder associated with chylomicronemia (CM) and an increased risk of pancreatitis. Most individuals with CM do not have FCS but exhibit multifactorial CM (MCM), which differs from FCS in terms of risk and disease management. This study aimed to inv...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278277/ https://www.ncbi.nlm.nih.gov/pubmed/32537545 http://dx.doi.org/10.1210/jendso/bvaa056 |