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Cellular mechanisms of heterogeneity in NF2-mutant schwannoma
Schwannomas are common sporadic tumors and hallmarks of familial neurofibromatosis type 2 (NF2) that develop predominantly on cranial and spinal nerves. Virtually all schwannomas result from inactivation of the NF2 tumor suppressor gene with few, if any, cooperating mutations. Despite their genetic...
Autores principales: | Chiasson-MacKenzie, Christine, Vitte, Jeremie, Liu, Ching-Hui, Wright, Emily A., Flynn, Elizabeth A., Stott, Shannon L., Giovannini, Marco, McClatchey, Andrea I. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030849/ https://www.ncbi.nlm.nih.gov/pubmed/36944680 http://dx.doi.org/10.1038/s41467-023-37226-0 |
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