Published January 1, 2023
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High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases
Creators
- Hiz, Ayse Semra
- Oktay, Yavuz
- Topf, Ana1
- Szabo, Nora2
- Serdal, Gungor3
- Yaramis, Ahmet4
- Sonmezler, Ece5
- Matalonga, Leslie6
- Yis, Uluc7
- Schon, Katherine
- Paramonov, Ida6
- Kalafatcilar, Ipek Polat
- Gao, Fei
- Rieger, Aliz8
- Arslan, Nur
- Yilmaz, Elmasnur5
- Ekinci, Burcu5
- Edem, Pinar Pulat7
- Aslan, Mahmut3
- Ozgor, Bilge3
- 1. Newcastle Univ, Inst Translat & Clin Res, John Walton Muscular Dystrophy Res Ctr, Newcastle Upon Tyne, Tyne & Wear, England
- 2. New St Johns Hosp & Northern Buda United Hosp, Epilepsy Neurol Polyclin Buda Childrens Hosp, Budapest, Hungary
- 3. Inonu Univ, Dept Paediat Neurol, Turgut Ozal Res Ctr, Fac Med, Malatya, Turkiye
- 4. Pediat Neurol Clin, Diyarbakir, Turkiye
- 5. Dokuz Eylul Univ, Izmir Int Biomed & Genome Inst, Izmir, Turkiye
- 6. Barcelona Inst Sci & Technol, Ctr Genom Regulat, CNAG CRG, Barcelona, Spain
- 7. Dokuz Eylul Univ, Sch Med, Dept Paediat Neurol, Izmir, Turkiye
- 8. Rehabil Ctr Physically Handicapped, Budapest, Hungary
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