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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Detaylı Bibliyografya
Yayımlandı:J Lipid Res
Asıl Yazarlar: Auclair, Nickolas, Sané, Alain T., Ahmarani, Lena, Patey, Nathalie, Beaulieu, Jean-François, Peretti, Noel, Spahis, Schohraya, Levy, Emile
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Biochemistry and Molecular Biology 2021
Konular:
Research Article
Online Erişim: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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