An unusual recurrent high-grade glioneuronal tumor with MAP2K1 mutation and CDKN2A/B homozygous deletion

Barry Cheaney, Stephen Bowden, Katie Krause, Emily A. Sloan, Arie Perry, David A. Solomon, Seunggu Jude Han, Matthew Wood

Research output: Contribution to journalLetter

Original languageEnglish (US)
Number of pages1
JournalActa Neuropathologica Communications
Volume7
Issue number1
DOIs
StatePublished - Jul 9 2019

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Mutation
Neoplasms

Keywords

  • Anaplastic
  • CDKN2A/B homozygous deletion
  • Glioneuronal tumor
  • MAP2K1 mutation
  • Multinodular and vacuolating neuronal tumor of the cerebrum
  • Next-generation sequencing

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Clinical Neurology
  • Cellular and Molecular Neuroscience

Cite this

An unusual recurrent high-grade glioneuronal tumor with MAP2K1 mutation and CDKN2A/B homozygous deletion. / Cheaney, Barry; Bowden, Stephen; Krause, Katie; Sloan, Emily A.; Perry, Arie; Solomon, David A.; Han, Seunggu Jude; Wood, Matthew.

In: Acta Neuropathologica Communications, Vol. 7, No. 1, 09.07.2019.

Research output: Contribution to journalLetter

Cheaney, Barry ; Bowden, Stephen ; Krause, Katie ; Sloan, Emily A. ; Perry, Arie ; Solomon, David A. ; Han, Seunggu Jude ; Wood, Matthew. / An unusual recurrent high-grade glioneuronal tumor with MAP2K1 mutation and CDKN2A/B homozygous deletion. In: Acta Neuropathologica Communications. 2019 ; Vol. 7, No. 1.
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AU - Solomon, David A.

AU - Han, Seunggu Jude

AU - Wood, Matthew

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