-
1
المؤلفون: Bhuwan, Khatri, Kandice L, Tessneer, Astrid, Rasmussen, Farhang, Aghakhanian, Tove Ragna, Reksten, Adam, Adler, Ilias, Alevizos, Juan-Manuel, Anaya, Lara A, Aqrawi, Eva, Baecklund, Johan G, Brun, Sara Magnusson, Bucher, Maija-Leena, Eloranta, Fiona, Engelke, Helena, Forsblad-d'Elia, Stuart B, Glenn, Daniel, Hammenfors, Juliana, Imgenberg-Kreuz, Janicke Liaaen, Jensen, Svein Joar Auglænd, Johnsen, Malin V, Jonsson, Marika, Kvarnström, Jennifer A, Kelly, He, Li, Thomas, Mandl, Javier, Martín, Gaétane, Nocturne, Katrine Brække, Norheim, Øyvind, Palm, Kathrine, Skarstein, Anna M, Stolarczyk, Kimberly E, Taylor, Maria, Teruel, Elke, Theander, Swamy, Venuturupalli, Daniel J, Wallace, Kiely M, Grundahl, Kimberly S, Hefner, Lida, Radfar, David M, Lewis, Donald U, Stone, C Erick, Kaufman, Michael T, Brennan, Joel M, Guthridge, Judith A, James, R Hal, Scofield, Patrick M, Gaffney, Lindsey A, Criswell, Roland, Jonsson, Per, Eriksson, Simon J, Bowman, Roald, Omdal, Lars, Rönnblom, Blake, Warner, Maureen, Rischmueller, Torsten, Witte, A Darise, Farris, Xavier, Mariette, Marta E, Alarcon-Riquelme, Caroline H, Shiboski, Marie, Wahren-Herlenius, Wan-Fai, Ng, Kathy L, Sivils, Indra, Adrianto, Gunnel, Nordmark, Christopher J, Lessard
المصدر: Nature communications. 13(1)
مصطلحات موضوعية: Sjogren's Syndrome, Humans, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Genome-Wide Association Study