Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT

Intraventricular meningiomas (IVMs) account for less than 5% of all intracranial meningiomas; hence their molecular phenotype remains unknown. In this study, we were interested whether genetic alterations in IVMs differ from meningiomas in other locations and analyzed our institutional series with r...

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Vydáno v:Acta Neuropathol Commun
Hlavní autoři: Jungwirth, Gerhard, Warta, Rolf, Beynon, Christopher, Sahm, Felix, von Deimling, Andreas, Unterberg, Andreas, Herold-Mende, Christel, Jungk, Christine
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2019
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6716845/
https://ncbi.nlm.nih.gov/pubmed/31470906
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-019-0793-4
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