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
| Autor: | Torres-Martín, Miguel, Kusak, M. Elena, Isla, Alberto, Burbano, Rommel R., Pinto, Giovanny R., Melendez, Barbara, Castresana, Javier S., Rey, Juan A. |
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| Zdroj: | In Cancer Genetics June 2015 208(6):327-332 |
| Databáze: | ScienceDirect |
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