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Article

Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas.

Journal of medical genetics - 1 Feb 2011

Christiaans I, Kenter S B, Brink H C, van Os T A M, Baas F, van den Munckhof P, Kidd A M J, Hulsebos T J M

Abstract excerpt

BACKGROUND: Multiple meningiomas occur in <10% of meningioma patients. Their development may be caused by the presence of a predisposing germline mutation in the neurofibromatosis type 2 (NF2) gene. The predisposing gene in patients with non-NF2 associated multiple meningiomas remains to be identified. Recently, SMARCB1 was reported to be a potential predisposing gene for multiple meningiomas in a family with...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20930055
DOI: 10.1136/jmg.2010.082420

Genes

SMARCB1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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