Sar1b mutant mice recapitulate gastrointestinal abnormalities associated with chylomicron retention disease

Chylomicron retention disease (CRD) is an autosomal recessive disorder associated with biallelic Sar1b mutations leading to defects in intracellular chylomicron (CM) trafficking and secretion. To date, a direct cause-effect relationship between CRD and Sar1b mutation has not been established, but ge...

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Detalhes bibliográficos
Publicado no:J Lipid Res
Main Authors: Auclair, Nickolas, Sané, Alain T., Ahmarani, Lena, Patey, Nathalie, Beaulieu, Jean-François, Peretti, Noel, Spahis, Schohraya, Levy, Emile
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2021
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8175419/
https://ncbi.nlm.nih.gov/pubmed/33964306
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jlr.2021.100085
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