The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis

Schwannomatosis is characterized by the predisposition to develop multiple schwannomas and, less commonly, meningiomas. Despite the clinical overlap with neurofibromatosis type 2 (NF2), schwannomatosis is not caused by germline NF2 gene mutations. Instead, germline mutations of either the SMARCB1 or...

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Detalles Bibliográficos
Autores principales: Kehrer-Sawatzki, Hildegard, Farschtschi, Said, Mautner, Victor-Felix, Cooper, David N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5258795/
https://www.ncbi.nlm.nih.gov/pubmed/27921248
http://dx.doi.org/10.1007/s00439-016-1753-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5258795/
https://www.ncbi.nlm.nih.gov/pubmed/27921248
http://dx.doi.org/10.1007/s00439-016-1753-8

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