Whole exome sequencing in a case of sporadic multiple meningioma reveals shared NF2, FAM109B, and TPRXL mutations, together with unique SMARCB1 alterations in a subset of tumor nodules.
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| Description | scientific article published on 11 April 2015 |
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author: Giovanny R Pinto Javier S. Castresana Miguel Torres-Martín Barbara Melendez |
| Publication date | April 11, 2015 |
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