A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening

Childhood meningiomas are rare. Recently, a new hereditary tumor predisposition syndrome has been discovered, resulting in an increased risk for spinal and intracranial clear cell meningiomas (CCMs) in young patients. Heterozygous loss-of-function germline mutations in the SMARCE1 gene are causative...

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Detalles Bibliográficos
Autores principales: Gerkes, E. H., Fock, J. M., den Dunnen, W. F. A., van Belzen, M. J., van der Lans, C. A., Hoving, E. W., Fakkert, I. E., Smith, M. J., Evans, D. G., Olderode-Berends, M. J. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794526/
https://www.ncbi.nlm.nih.gov/pubmed/26803492
http://dx.doi.org/10.1007/s10048-015-0472-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794526/
https://www.ncbi.nlm.nih.gov/pubmed/26803492
http://dx.doi.org/10.1007/s10048-015-0472-y

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