Solute carrier family 2 member 1 is involved in the development of nonalcoholic fatty liver disease.

doi:10.1002/hep.26052

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Article

Solute carrier family 2 member 1 is involved in the development of nonalcoholic fatty liver disease.

Hepatology (Baltimore, Md.) - 1 Feb 2013

Vazquez-Chantada Mercedes, Gonzalez-Lahera Aintzane, Martinez-Arranz Ibon, Garcia-Monzon Carmelo, Regueiro Manuela M, Garcia-Rodriguez Juan L, Schlangen Karin A, Mendibil Iñaki, Rodriguez-Ezpeleta Naiara, Lozano Juan J, Banasik Karina, Justesen Johanne M, Joergensen Torben, Witte Daniel R, Lauritzen Torsten, Hansen Torben, Pedersen Oluf, Veyrie Nicolas, Clement Karine, Tordjman Joan, Tran Albert, Le Marchand-Brustel Yannik, Buque Xabier, Aspichueta Patricia, Echevarria-Uraga Jose J, Martin-Duce Antonio, Caballeria Joan, Gual Philippe, Castro Azucena, Mato Jose M, Martinez-Chantar Maria L, Aransay Ana M

Abstract excerpt

UNLABELLED: Susceptibility to develop nonalcoholic fatty liver disease (NAFLD) has genetic bases, but the associated variants are uncertain. The aim of the present study was to identify genetic variants that could help to prognose and further understand the genetics and development of NAFLD. Allele frequencies of 3,072 single-nucleotide polymorphisms (SNPs) in 92 genes were characterized in 69 NAFLD patients and...

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PMID: 22961556
DOI: 10.1002/hep.26052

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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