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Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families

Title:	Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families
Authors:	Büyükgöl, Furkan^Aff1; Gürdamar, Berk^Aff1; Aluçlu, Mehmet Ufuk^Aff2; Beckmann, Yeşim^Aff3; Bilguvar, Kaya^{Aff4, Aff5}; Boz, Cavit^Aff6; Bülbül, Alper^Aff1; Bünül, Sena Destan^Aff7; Çetin, Özge^Aff8; Demir, Caner Feyzi^Aff9; Demir, Serkan^Aff10; Duman, Taşkın^Aff11; Efendi, Hüsnü^Aff7; Ekmekçi, Özgül^Aff12; Ertetik, Utku^Aff13; Ethemoğlu, Özlem^Aff14; Everest, Elif^Aff15; Gümüş, Haluk^Aff16; Gündüz, Tuncay^Aff17; Karabudak, Rana^Aff18; Karaman, Bedriye^Aff12; Kürtüncü, Murat^Aff17; Mutluer, Muzaffer^Aff19; Reda, Meziyet Dilara^Aff20; Saip, Sabahattin^Aff21; Seferoğlu, Meral^Aff22; Sever, Elif^Aff1; Sezerman, Osman Ugur^Aff1; Şen, Sedat^Aff23; Taşdelen, Beril^Aff10; Tecellioğlu, Mehmet^Aff24; Terzi, Murat^Aff23; Tuncer, Aslı^Aff25; Turan, Ömer Faruk^Aff26; Tütüncü, Melih^Aff21; Uncu, Gülgün^Aff27; Uygunoğlu, Uğur^Aff21; Uzunköprü, Cihat^Aff3; Voyvoda, Umut^Aff20; Yetkin, Mehmet Fatih^Aff28; Yüceyar, Nur^Aff12; Siva, Aksel^{Aff21, IDs4159802594691x_cor1}; Turanlı, Eda Tahir^{Aff8, Aff20, IDs4159802594691x_cor2}
Source:	Scientific Reports. 15(1)
Database:	Springer Nature Journals