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Identification and characterization of a novel DGAT1 missense mutation associated with congenital diarrhea

Acyl-CoA:diacylglycerol acyltransferase (DGAT)1 and DGAT2 catalyze triglyceride (TG) biosynthesis in humans. Biallelic loss-of-function mutations in human DGAT1 result in severe congenital diarrhea and protein-losing enteropathy. Additionally, pharmacologic inhibition of DGAT1 led to dose-related di...

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Detalles Bibliográficos
Autores principales:	Gluchowski, Nina L., Chitraju, Chandramohan, Picoraro, Joseph A., Mejhert, Niklas, Pinto, Shirly, Xin, Winnie, Kamin, Daniel S., Winter, Harland S., Chung, Wendy K., Walther, Tobias C., Farese, Robert V.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The American Society for Biochemistry and Molecular Biology 2017
Materias:	Patient-Oriented and Epidemiological Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454518/ https://www.ncbi.nlm.nih.gov/pubmed/28373485 http://dx.doi.org/10.1194/jlr.P075119

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