High frequency of the PNPLA3 rs738409 [G] single-nucleotide polymorphism in Hmong individuals as a potential basis for a predisposition to chronic liver disease.

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Title: High frequency of the PNPLA3 rs738409 [G] single-nucleotide polymorphism in Hmong individuals as a potential basis for a predisposition to chronic liver disease.
Authors: Tepper CG; Department of Biochemistry and Molecular Medicine, University of California Davis, Sacramento, California., Dang JHT; Division of Hematology and Oncology, Department of Internal Medicine, University of California Davis, Sacramento, California., Stewart SL; Division of Biostatistics, Department of Public Health Sciences, University of California Davis, Sacramento, California., Fang DM; Hmong Cultural Center of Butte County, Oroville, California., Wong KA; Department of Internal Medicine, University of California Davis, Sacramento, California., Liu SY; Department of Pathology and Laboratory Medicine, University of California Davis, Sacramento, California., Davis RR; Department of Pathology and Laboratory Medicine, University of California Davis, Sacramento, California., Dao DY; Division of Digestive and Liver Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas., Gregg JP; Department of Pathology and Laboratory Medicine, University of California Davis, Sacramento, California., Török NJ; Department of Internal Medicine, University of California Davis, Sacramento, California., Chen MS Jr; Division of Hematology and Oncology, Department of Internal Medicine, University of California Davis, Sacramento, California.
Source: Cancer [Cancer] 2018 Apr 01; Vol. 124 Suppl 7, pp. 1583-1589.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 0374236 Publication Model: Print Cited Medium: Internet ISSN: 1097-0142 (Electronic) Linking ISSN: 0008543X NLM ISO Abbreviation: Cancer
Database: MEDLINE Ultimate
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Description
ISSN:1097-0142
DOI:10.1002/cncr.31122