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Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

Developmental AnomalyRare DiseasesSomatic VariantMendelian DisorderGenetic DisorderGeneticsPathologyLztr1 PredisposeMolecular GeneticsDisease Gene IdentificationGermline Loss-of-function MutationsNeuropathologyMedicineMultiple SchwannomasClinical Genetics