Familial unilateral vestibular schwannoma is rarely caused by inherited variants in the NF2 gene

OBJECTIVES/HYPOTHESIS: Unilateral vestibular schwannoma (VS) occurs with a lifetime risk of around 1 in 1,000 and is due to inactivation of the NF2 gene, either somatically or from a constitutional mutation. It has been postulated that familial occurrence of unilateral VS occurs more frequently than...

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Detalhes bibliográficos
Publicado no:Laryngoscope
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
Assuntos:
Otology/Neurotology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6563429/
https://ncbi.nlm.nih.gov/pubmed/30325044
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/lary.27554
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