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Autor:
Encarna Guillén-Navarro, Ann Nordgren, Agne Liedén, Ronnie Wright, Chiara Pantaleoni, María Juliana Ballesta-Martínez, Philippe M. Campeau, Meriel McEntagart, Katherine E. Schertz, Céline Pebrel-Richard, Silvia Annunziata, Megan Thomas, Peter E. Clayton, Cristina Hernando, Catherine Sarret, Paul R. Kasher, Bronwyn Kerr, Tiziana Granata, Jennifer L. Eaton, Caroline E. Laverriere, Francesca L. Sciacca, Eric Glasgow, Adam Jackson, Olaya Villa-Marcos, Siddharth Banka
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2016, 98 (2), pp.363-372. ⟨10.1016/j.ajhg.2015.12.014⟩
American Journal of Human Genetics, 2016, 98 (2), pp.363-372. ⟨10.1016/j.ajhg.2015.12.014⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2016, 98 (2), pp.363-372. ⟨10.1016/j.ajhg.2015.12.014⟩
American Journal of Human Genetics, 2016, 98 (2), pp.363-372. ⟨10.1016/j.ajhg.2015.12.014⟩
Genetic studies of intellectual disability and identification of monogenic causes of obesity in humans have made immense contribution toward the understanding of the brain and control of body mass. The leptin > melanocortin > SIM1 pathway is dysregul