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Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants

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Main Authors: Hutter, Sonja (Author) , Piro, Rosario M. (Author) , Reuss, David (Author) , Hovestadt, Volker (Author) , Sahm, Felix (Author) , Farschtschi, Said (Author) , Kehrer-Sawatzki, Hildegard (Author) , Wolf, Stephan (Author) , Lichter, Peter (Author) , Deimling, Andreas von (Author) , Schuhmann, Martin U. (Author) , Pfister, Stefan (Author) , Jones, David T. W. (Author) , Mautner, Victor F. (Author)
Format: Article (Journal)
Language:English
Published: 10 July 2014
In: Acta neuropathologica
Year: 2014, Volume: 128, Issue: 3, Pages: 449-452
ISSN:1432-0533
DOI:10.1007/s00401-014-1311-1
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s00401-014-1311-1
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Author Notes: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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Item Description:Gesehen am 22.07.2020
Physical Description:Online Resource
ISSN:1432-0533
DOI:10.1007/s00401-014-1311-1

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