Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants - Hutter, Sonja; Piro, Rosario M.; Reuss, David; Hovestadt, Volker; Sahm, Felix; Farschtschi, Said; Kehrer-Sawatzki, Hildegard; Wolf, Stephan; Lichter, Peter; Deimling, Andreas von; Schuhmann, Martin U.; Pfister, Stefan; et al. (Acta neuropathologica, 2014)
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