Recurrent EGFR alterations in NTRK3 fusion negative congenital mesoblastic nephroma

OBJECTIVES: To identify oncogenic driver mutations in congenital mesoblastic nephroma (CMN) cases lacking ETV6-NTRK3 fusion and discuss their diagnostic value. DESIGN: The institutional pathology database was queried for cases with a morphologic diagnosis of CMN. Cases positive for ETV6 rearrangemen...

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Detalles Bibliográficos
Autores principales: Lei, Li, Stohr, Bradley A., Berry, Stacey, Lockwood, Christina M., Davis, Jessica L., Rudzinski, Erin R., Kunder, Christian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260589/
https://www.ncbi.nlm.nih.gov/pubmed/32490123
http://dx.doi.org/10.1016/j.plabm.2020.e00164

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260589/
https://www.ncbi.nlm.nih.gov/pubmed/32490123
http://dx.doi.org/10.1016/j.plabm.2020.e00164

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