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A Human REPIN1 Gene Variant: Genetic Risk Factor for the Development of Nonalcoholic Fatty Liver Disease
OBJECTIVES: We tested the hypothesis that a genetic deletion (Del) variant in the REPIN1 gene is associated with the severity of nonalcoholic fatty liver disease (NAFLD) in humans. METHODS: Sixty-three donors of liver biopsies from individuals with obesity and different degrees of NAFLD and fibrosis...
Autores principales: | Abshagen, Kerstin, Berger, Claudia, Dietrich, Arne, Schütz, Tatjana, Wittekind, Christian, Stumvoll, Michael, Blüher, Matthias, Klöting, Nora |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056046/ https://www.ncbi.nlm.nih.gov/pubmed/31922994 http://dx.doi.org/10.14309/ctg.0000000000000114 |
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