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

@article{VzquezChantada2013SoluteCF,
  title={Solute carrier family 2 member 1 is involved in the development of nonalcoholic fatty liver disease.},
  author={Mercedes V{\'a}zquez-Chantada and Aintzane Gonzalez-Lahera and Ibon Mart{\'i}nez-Arranz and Carmelo Garc{\'i}a-Monz{\'o}n and Manuela M Regueiro and Juan Lu{\'i}s Garc{\'i}a-Rodr{\'i}guez and Karin A Schlangen and I{\~n}aki Mendibil and Naiara Rodr{\'i}guez-Ezpeleta and Juan Jos{\'e} Lozano and Karina Banasik and Johanne Marie Justesen and T. J. D. Joergensen and Daniel Witte and T Lauritzen and Torben Hansen and Oluf Pedersen and Nicolas Veyrie and Karine Cl{\'e}ment and Joan Tordjman and Albert Tran and Yannik Le Marchand-Brustel and Xabier Buqu{\'e} and Patricia Aspichueta and Jos{\'e} Javier Echevarria-Uraga and Antonio Mart{\'i}n-Duce and Joan Caballer{\'i}a and Philippe Gual and Azucena Castro and Jose M. Mato and Mar{\'i}a L. Mart{\'i}nez-Chantar and Ana M. Aransay},
  journal={Hepatology},
  year={2013},
  volume={57 2},
  pages={505-14}
}
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 217 healthy individuals. The markers that showed significant allele-frequency… CONTINUE READING
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