Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants
Gespeichert in:
| Hauptverfasser: | , , , , , , , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
10 July 2014
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| In: |
Acta neuropathologica
Year: 2014, Jahrgang: 128, Heft: 3, Pages: 449-452 |
| ISSN: | 1432-0533 |
| DOI: | 10.1007/s00401-014-1311-1 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s00401-014-1311-1
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| Verfasserangaben: | Sonja Hutter · Rosario M. Piro · David E. Reuss · Volker Hovestadt · Felix Sahm · Said Farschtschi · Hildegard Kehrer-Sawatzki · Stephan Wolf · Peter Lichter · Andreas von Deimling · Martin U. Schuhmann · Stefan M. Pfister · David T.W. Jones · Victor F. Mautner |
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