High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases
Semra Hız Kurul(Dokuz Eylül University), Rita Horváth(Wellcome Centre for Mitochondrial Research), Nur Arslan(Dokuz Eylül University), Nóra Szabó(Buda Health Center), Katherine Schon(University of Cambridge), Uluç Yiş(Dokuz Eylül University), Patrick F. Chinnery(Wellcome Centre for Mitochondrial Research), Denisa Hathazi(University of Cambridge), Serdal Güngör(Inonu University), Elmasnur Yilmaz(Dokuz Eylül University), Yavuz Oktay(Dokuz Eylül University), Leslie Matalonga(Centre for Genomic Regulation), Kiran Polavarapu(University of Ottawa), Hanns Lochmüller(Muscular Dystrophy UK), Ashwati Nair(King's College London), Aliz Rieger, Sergi Beltrán(Centro Nacional de Análisis Genómico), Mahmut Aslan(Inonu University), Fei Gao(University of Cambridge), Ana Töpf(NIHR Newcastle Biomedical Research Centre), İpek Polat Kalafatcilar(Dokuz Eylül University), Alysia Kern Lovgren(Broad Institute), Ece Sönmezler(Dokuz Eylül University), Bilge Özgör(Inonu University), Angela Lochmüller(King's College London), Emily O’Heir(MACOM (United States)), Henry Houlden(University College London), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Ida Paramonov(Universitat Pompeu Fabra), Steven Laurie(Centre for Genomic Regulation), Ahmet Yaramış(Diyarbakır Askeri Hastanesi), Andreas Roos(University of Ottawa), Pınar Edem(Dokuz Eylül University), Juliane Müller(University of Cambridge), Burcu Ekinci(Dokuz Eylül University)
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