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

  • 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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Abstract

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Bibliographical data

Original languageEnglish
ISSN0001-6322
DOIs
Publication statusPublished - 01.09.2014
PubMed 25008767