Somatic SMARCB1 Mutation in Sporadic Multiple Meningiomas: Case Report

Somatic SMARCB1 Mutation in Sporadic Multiple Meningiomas: Case Report

Background: Multiple intracranial meningiomas account for <10% of all meningiomas. Familial multiple meningiomas have been linked to germline mutations in two genes: neurofibromatosis type 2 (NF2) and SWIch/Sucrose Non-Fermentable (SWI/SNF)-related matrix-associated actin-dependent regulator...

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Bibliographic Details
Main Authors: Alice S. Wang, Ali O. Jamshidi, Nathan Oh, Ronald Sahyouni, Behdokht Nowroozizadeh, Ronald Kim, Frank P. K. Hsu, Daniela Bota
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-10-01
Series:Frontiers in Neurology
Subjects:
sporadic multiple meningiomas
familial multiple meningiomas
SMARCB1
NF2
somatic mutation
germline mutation
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2018.00919/full

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https://www.frontiersin.org/article/10.3389/fneur.2018.00919/full

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