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

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Title: Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.
Authors: Büyükgöl, Furkan1 (AUTHOR), Gürdamar, Berk1 (AUTHOR), Aluçlu, Mehmet Ufuk2 (AUTHOR), Beckmann, Yeşim3 (AUTHOR), Bilguvar, Kaya4,5 (AUTHOR), Boz, Cavit6 (AUTHOR), Bülbül, Alper1 (AUTHOR), Bünül, Sena Destan7 (AUTHOR), Çetin, Özge8 (AUTHOR), Demir, Caner Feyzi9 (AUTHOR), Demir, Serkan10 (AUTHOR), Duman, Taşkın11 (AUTHOR), Efendi, Hüsnü7 (AUTHOR), Ekmekçi, Özgül12 (AUTHOR), Ertetik, Utku13 (AUTHOR), Ethemoğlu, Özlem14 (AUTHOR), Everest, Elif15 (AUTHOR), Gümüş, Haluk16 (AUTHOR), Gündüz, Tuncay17 (AUTHOR), Karabudak, Rana18 (AUTHOR)
Source: Scientific Reports. 4/5/2025, Vol. 15 Issue 1, p1-14. 14p.
Database: Academic Search Ultimate
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PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=184262704
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