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...

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Detalles Bibliográficos
Autores principales: Tremblay, Karine, Gaudet, Daniel, Khoury, Etienne, Brisson, Diane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Brief Report
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

Internet

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

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