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HSD17B13 truncated variant is associated with a mild hepatic phenotype in Wilson’s Disease
HSD17B13 encodes hydroxysteroid 17-β dehydrogenase 13, a novel liver lipid-droplet associated protein that is involved in the regulation of lipid biosynthetic processes. A protein-truncating HSD17B13 variant (rs72613567) was shown to protect individuals from alcoholic and non-alcoholic liver disease...
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| Vydáno v: | JHEP Rep |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7001574/ https://ncbi.nlm.nih.gov/pubmed/32039348 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jhepr.2019.02.007 |
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