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

Gessi, Marco

MET T992I mutation in a case of ependymoblastoma/embryonal tumour with multilayered rosettes. [electronic resource] - Journal of clinical pathology Nov 2014 - 1017-8 p. digital

Publication Type: Case Reports; Letter

1472-4146

10.1136/jclinpath-2014-202563 doi


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