New developments in neurofibromatosis type 2 and vestibular schwannoma

Neurofibromatosis type 2 (NF2) is a rare autosomal dominant disorder characterized by the development of multiple nervous system tumors due to mutation in the NF2 tumor suppressor gene. The hallmark feature of the NF2 syndrome is the development of bilateral vestibular schwannomas (VS). Although the...

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Detalles Bibliográficos
Autores principales: Ren, Yin, Chari, Divya A, Vasilijic, Sasa, Welling, D Bradley, Stankovic, Konstantina M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881257/
https://www.ncbi.nlm.nih.gov/pubmed/33604573
http://dx.doi.org/10.1093/noajnl/vdaa153

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881257/
https://www.ncbi.nlm.nih.gov/pubmed/33604573
http://dx.doi.org/10.1093/noajnl/vdaa153

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