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Familial unilateral vestibular schwannoma is rarely caused by inherited variants in the NF2 gene.
Evans, D Gareth; Wallace, Andrew J; Hartley, Claire; Freeman, Simon R; Lloyd, Simon K; Thomas, Owen; Axon, Patrick; Hammerbeck-Ward, Charlotte L; Pathmanaban, Omar; Rutherford, Scott A; Kellett, Mark; Laitt, Roger; King, Andrew T; Bischetsrieder, Jemma; Blakeley, Jaishri; Smith, Miriam J.
Afiliação
  • Evans DG; Department of Genomic Medicine, Manchester, United Kingdom.
  • Wallace AJ; Department of Genomic Medicine, Manchester, United Kingdom.
  • Hartley C; Department of Genomic Medicine, Manchester, United Kingdom.
  • Freeman SR; Department of Otolaryngology, University of Manchester, Manchester Academic Health Science Centre, Division of Evolution and Genomic Sciences, Manchester Universities NHS Foundation Trust, Manchester, United Kingdom.
  • Lloyd SK; Department of Otolaryngology, University of Manchester, Manchester Academic Health Science Centre, Division of Evolution and Genomic Sciences, Manchester Universities NHS Foundation Trust, Manchester, United Kingdom.
  • Thomas O; Department of NeuroRadiology, Salford Royal NHS Foundation Trust, Salford, Manchester, United Kingdom.
  • Axon P; Department of Otolaryngology, Addenbrooke's Hospital Cambridge, United Kingdom.
  • Hammerbeck-Ward CL; Department of Neurosurgery, Salford Royal NHS Foundation Trust, Salford, Manchester, United Kingdom.
  • Pathmanaban O; Department of Neurosurgery, Salford Royal NHS Foundation Trust, Salford, Manchester, United Kingdom.
  • Rutherford SA; Department of Neurosurgery, Salford Royal NHS Foundation Trust, Salford, Manchester, United Kingdom.
  • Kellett M; Department of Neurology, Salford Royal NHS Foundation Trust, Salford, Manchester, United Kingdom.
  • Laitt R; Department of NeuroRadiology, Salford Royal NHS Foundation Trust, Salford, Manchester, United Kingdom.
  • King AT; Department of Neurosurgery, Salford Royal NHS Foundation Trust, Salford, Manchester, United Kingdom.
  • Bischetsrieder J; Department of Genetics, Kaiser Permanente, Fontana, California, U.S.A.
  • Blakeley J; Johns Hopkins Hospital, Baltimore, Maryland, U.S.A.
  • Smith MJ; Department of Genomic Medicine, Manchester, United Kingdom.
Laryngoscope ; 129(4): 967-973, 2019 04.
Article em En | MEDLINE | ID: mdl-30325044
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuroma Acústico / Genes da Neurofibromatose 2 Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Humans / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuroma Acústico / Genes da Neurofibromatose 2 Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Humans / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article