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High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases.
Semra Hiz Kurul, Yavuz Oktay, Ana Töpf, Nóra Zs Szabó, Serdal Güngör, Ahmet Yaramis, Ece Sonmezler, Leslie Matalonga, Uluc Yis, Katherine Schon, Ida Paramonov, İpek Polat Kalafatcilar, Fei Gao, Aliz Rieger, Nur Arslan, Elmasnur Yilmaz, Burcu Ekinci, Pinar Pulat Edem, Mahmut Aslan, Bilge Özgör, Angela Lochmüller, Ashwati Nair, Emily O'Heir, Alysia K Lovgren, Broad Center for Mendelian Genomics, Reza Maroofian, Henry Houlden, Kiran Polavarapu, Andreas Roos, Juliane S Müller, Denisa Hathazi, Patrick F Chinnery, Steven Laurie, Sergi Beltran, Hanns Lochmüller, Rita Horvath
OAI: oai:www.repository.cam.ac.uk:1810/329391 • DOI: 10.17863/CAM.76839