NF2/Merlin in hereditary neurofibromatosis 2 versus cancer: biologic mechanisms and clinical associations

Inactivating germline mutations in the tumor suppressor gene NF2 cause the hereditary syndrome neurofibromatosis 2, which is characterized by the development of neoplasms of the nervous system, most notably bilateral vestibular schwannoma. Somatic NF2 mutations have also been reported in a variety o...

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Detalles Bibliográficos
Autores principales: Schroeder, Rebecca Dunbar, Angelo, Laura S., Kurzrock, Razelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960189/
https://www.ncbi.nlm.nih.gov/pubmed/24393766

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960189/
https://www.ncbi.nlm.nih.gov/pubmed/24393766

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