Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants
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| Description | article published in 2014 |
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author: Stefan M. Pfister Andreas von Deimling David T. W. Jones Felix Sahm Volker Hovestadt Rosario M. Piro Peter Lichter Martin U Schuhmann Victor-Felix Mautner Hildegard Kehrer-Sawatzki David E Reuss Sonja Hutter |
| Publication date | July 10, 2014 |
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