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A Fluorescence-based Assay for Characterization and Quantification of Lipid Droplet Formation in Human Intestinal Organoids
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Neutral lipid storage disease: genetic disorders caused by mutations in adipose triglyceride lipase/PNPLA2 or

Martina Schweiger1, Achim Lass, Robert Zimmermann

  • 1Institute of Molecular Biosciences, University of Graz, Graz, Austria.

American Journal of Physiology. Endocrinology and Metabolism
|April 30, 2009
PubMed

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