Volanesorsen: A New Era in the Treatment of Severe Hypertriglyceridemia

Introduction: Familial chylomicronemia syndrome (FCS) is a rare inherited disease, mainly due to lipoprotein lipase (LPL) gene mutations, leading to lipid abnormalities. Volanesorsen, a second-generation 2′-O-methoxyethyl (2′-MOE) chimeric antisense therapeutic oligonucleotide, can decrease plasma a...

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Detalles Bibliográficos
Autores principales: Kolovou, Genovefa, Kolovou, Vana, Katsiki, Niki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880470/
https://www.ncbi.nlm.nih.gov/pubmed/35207255
http://dx.doi.org/10.3390/jcm11040982

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880470/
https://www.ncbi.nlm.nih.gov/pubmed/35207255
http://dx.doi.org/10.3390/jcm11040982

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