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

Sadeleştirilmiş öğe sayfası
dc.contributor.authorBuyukgol, Furkan
dc.contributor.authorGurdamar, Berk
dc.contributor.authorAluclu, Mehmet Ufuk
dc.contributor.authorBeckmann, Yesim
dc.contributor.authorBilguvar, Kaya
dc.contributor.authorBoz, Cavit
dc.contributor.authorBulbul, Alper
dc.contributor.authorBunul, Sena Destan
dc.contributor.authorCetin, Ozge
dc.contributor.authorDemir, Caner Feyzi
dc.contributor.authorDemir, Serkan
dc.contributor.authorDuman, Taskin
dc.contributor.authorEfendi, Huesnue
dc.contributor.authorEkmekci, Ozgul
dc.contributor.authorErtetik, Utku
dc.contributor.authorEthemoglu, Ozlem
dc.contributor.authorEverest, Elif
dc.contributor.authorGumus, Haluk
dc.contributor.authorGunduz, Tuncay
dc.contributor.authorKarabudak, Rana
dc.contributor.authorKaraman, Bedriye
dc.contributor.authorKurtuncu, Murat
dc.contributor.authorMutluer, Muzaffer
dc.contributor.authorReda, Meziyet Dilara
dc.contributor.authorSaip, Sabahattin
dc.contributor.authorSeferoglu, Meral
dc.contributor.authorSever, Elif
dc.contributor.authorSezerman, Osman Ugur
dc.contributor.authorSen, Sedat
dc.contributor.authorTasdelen, Beril
dc.contributor.authorTecellioglu, Mehmet
dc.contributor.authorTerzi, Murat
dc.contributor.authorTuncer, Asli
dc.contributor.authorTuran, Omer Faruk
dc.contributor.authorTutuncu, Melih
dc.contributor.authorUncu, Gulgun
dc.contributor.authorUygunoglu, Ugur
dc.contributor.authorUzunkopru, Cihat
dc.contributor.authorVoyvoda, Umut
dc.contributor.authorYetkin, Mehmet Fatih
dc.contributor.authorYuceyar, Nur
dc.contributor.authorSiva, Aksel
dc.contributor.authorTuranli, Eda Tahir
dc.date.accessioned2025-10-16T15:11:52Z
dc.date.issued2025
dc.identifier.doi10.1038/s41598-025-94691-x
dc.identifier.otherWOS:001460360100012
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5079
dc.publisherNATURE PORTFOLIO
dc.sourceSCIENTIFIC REPORTS
dc.subjectGenetics
dc.subjectFamilial multiple sclerosis
dc.subjectBlood\\-brain barrier
dc.subjectWhole exome sequencing
dc.titleExome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families
dc.typeArticle

Dosyalar

Orijinal seri

Şimdi gösteriliyor 1 - 1 / 1
Thumbnail Image
Ad:
Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in.pdf
Boyut:
2.35 MB
Format:
Adobe Portable Document Format
İndir

Koleksiyonlar

WOS