RARE-15. Astroblastoma, MN1 altered comprises two molecularly and clinically distinct subgroups defined by the fusion partners BEND2 and CXXC5

In the recent 5th edition of the WHO classification of CNS tumors, ‘Astroblastoma, MN1 altered’ is recognized a distinct brain tumor type, occurring in children and young adults. Due to its rarity and novelty, little is known about clinical and molecular traits. Therefore, we initiated an internatio...

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Detalles Bibliográficos
Autores principales: Schmitt-Hoffner, Felix, Gojo, Johannes, Mauermann, Monika, von Hoff, Katja, Sill, Martin, Stichel, Damian, Capper, David, Tauziede-Espariat, Arnault, Varlet, Pascale, Aldape, Kenneth, Abdullaev, Zied, Donson, Andrew M, Schüller, Ulrich, Snuderl, Matija, Brandner, Sebastian, Łastowska, Maria, Trubicka, Joanna, Miele, Evelina, van der Lugt, Jasper, Bunt, Jens, Kramm, Christof, Zapotocky, Michal, Sahm, Felix, Korshunov, Andrey, Jäger, Natalie, Pfister, Stefan M, Kool, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Craniopharyngioma and Rare Tumors
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164977/
http://dx.doi.org/10.1093/neuonc/noac079.040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164977/
http://dx.doi.org/10.1093/neuonc/noac079.040

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