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...

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Detaylı Bibliyografya
Yayımlandı:Hepatology
Asıl Yazarlar: Brady, Graham F., Kwan, Raymond, Ulintz, Peter J., Nguyen, Phirum, Bassirian, Shirin, Basrur, Venkatesha, Nesvizhskii, Alexey I., Loomba, Rohit, Omary, M. Bishr
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2018
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Article
Online Erişim: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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