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Nuclear lamina genetic variants, including a truncated LAP2, in twins and siblings with nonalcoholic fatty liver disease

Nonalcoholic fatty liver disease (NAFLD) is becoming the major chronic liver disease in many countries. Its pathogenesis is multifactorial but twin and familial studies indicate significant heritability, which is not fully explained by currently-known genetic susceptibility loci. Notably, mutations...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Hepatology
Prif Awduron: Brady, Graham F., Kwan, Raymond, Ulintz, Peter J., Nguyen, Phirum, Bassirian, Shirin, Basrur, Venkatesha, Nesvizhskii, Alexey I., Loomba, Rohit, Omary, M. Bishr
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2018
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5849478/
https://ncbi.nlm.nih.gov/pubmed/28902428
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hep.29522
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