MET T992I mutation in a case of ependymoblastoma/embryonal tumour with multilayered rosettes

J Clin Pathol. 2014 Nov;67(11):1017-8. doi: 10.1136/jclinpath-2014-202563. Epub 2014 Sep 5.

Authors

Marco Gessi¹, Halil Demir¹, Tobias Goschzik¹, Torsten Pietsch¹

Affiliation

¹ Institute of Neuropathology, University of Bonn Medical Center, Bonn, Germany.

PMID: 25194039
DOI: 10.1136/jclinpath-2014-202563

No abstract available

Keywords: BRAIN TUMOURS; NEUROPATHOLOGY; ONCOGENES.

Publication types

Case Reports
Letter

MeSH terms

Biopsy
Child, Preschool
DNA Mutational Analysis
Female
Genetic Predisposition to Disease
Humans
Mutation*
Neuroectodermal Tumors, Primitive / enzymology
Neuroectodermal Tumors, Primitive / genetics*
Neuroectodermal Tumors, Primitive / pathology*
Neuroectodermal Tumors, Primitive / therapy
Phenotype
Proto-Oncogene Proteins c-met / genetics*
Supratentorial Neoplasms / enzymology
Supratentorial Neoplasms / genetics*
Supratentorial Neoplasms / pathology*
Supratentorial Neoplasms / therapy

Substances

MET protein, human
Proto-Oncogene Proteins c-met