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Animal model of Sar1b deficiency presents lipid absorption deficits similar to Anderson Disease
Anderson Disease (ANDD) or Chylomicron Retention Disease (CMRD) is a rare, hereditary lipid malabsorption syndrome associated with mutations in the SAR1B gene that is characterized by failure to thrive and hypocholesterolemia. Although the SAR1B structure has been resolved and its role in formation...
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| Foilsithe in: | J Mol Med (Berl) |
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| Main Authors: | , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4319984/ https://ncbi.nlm.nih.gov/pubmed/25559265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00109-014-1247-x |
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