The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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wetenschappelijk artikel

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наукова стаття, опублікована у вересні 2018

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The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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P1476

The Genetics of Clinical Liver Diseases: Insight into the E167K Variant

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P2093

Quanjiang Dong

http://www.w3.org/2001/XMLSchema#string

Shiying Xuan

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Shousheng Liu

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Xiaoyu Zhang

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Yongning Xin

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P2860

TM6SF2 is a regulator of liver fat metabolism influencing triglyceride secretion and hepatic lipid droplet content

Common variants at 30 loci contribute to polygenic dyslipidemia

Biological, clinical and population relevance of 95 loci for blood lipids

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

TM6SF2 E167K Variant, a Novel Genetic Susceptibility Variant, Contributing to Nonalcoholic Fatty Liver Disease

Management of hepatocellular carcinoma: An update

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Discovery and refinement of loci associated with lipid levels.

Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese.

Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease

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326-331

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P31

scholarly article

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10.14218/JCTH.2018.00022

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P407

English

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P478

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P577

2018-09-28T00:00:00Z

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30271746

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6160302

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