Genomic alterations in Turcot syndrome: Insights from whole exome sequencing

J Neurol Sci. 2020 Oct 15:417:117056. doi: 10.1016/j.jns.2020.117056. Epub 2020 Jul 25.

¹ Department of Neurology, Yale School of Medicine, New Haven, CT, United States of America; Department of Neurosurgery, Yale School of Medicine, New Haven, CT, United States of America; Department of Neurosurgery, Ludwig Maximilians University School of Medicine, Munich, Germany. Electronic address: p.karschnia@med.uni-muenchen.de.
² Department of Neurosurgery, Yale School of Medicine, New Haven, CT, United States of America. Electronic address: zeynep.erson@yale.edu.
³ Department of Pathology, Yale School of Medicine, New Haven, CT, United States of America. Electronic address: anita.huttner@yale.edu.
⁴ Department of Neurology, Yale School of Medicine, New Haven, CT, United States of America. Electronic address: leon.kaulen@yale.edu.
⁵ Department of Neurosurgery, Yale School of Medicine, New Haven, CT, United States of America. Electronic address: daniel.duran@yale.edu.
⁶ Department of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, United States of America. Electronic address: robert.fulbright@yale.edu.
⁷ Department of Neurosurgery, Yale School of Medicine, New Haven, CT, United States of America. Electronic address: murat.gunel@yale.edu.
⁸ Department of Neurology, Yale School of Medicine, New Haven, CT, United States of America; Department of Neurosurgery, Yale School of Medicine, New Haven, CT, United States of America. Electronic address: joachim.baehring@yale.edu.

No abstract available

Keywords: Genomics; Glioma; Mismatch repair deficiency; Sequencing; Tumorigenesis; Turcot syndrome.

Publication types