View in EDS HTML Full Text PDF Full Text

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

Saved in:
Bibliographic Details
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
Full text is not displayed to guests.
Description
ISSN:20452322
DOI:10.1038/s41598-025-94691-x