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

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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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Citations

12

References

2014

Year

Sonja Hutter, Rosario M. Piro, Volker Hovestadt, Felix Sahm, Said Farschtschi, Hildegard Kehrer‐Sawatzki, Stephan Wolf, Peter Lichter, Andreas von Deimling, Martin U. Schuhmann,

Acta Neuropathologica

Neuro-oncologySchwannomatosis CasesMendelian DisorderGenetic DisorderMedicineGeneticsPathologyMolecular PathologyDisease Gene IdentificationNeuropathologyMolecular DiagnosticsVariant InterpretationLztr1 Germline Variants

References

	Year	Citations

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