The SH3PXD2A-HTRA1 fusion transcript is extremely rare in Norwegian sporadic vestibular schwannoma patients

INTRODUCTION: Vestibular schwannoma (VS) is a benign intracranial tumor in which the underlying genetics is largely uncertain, apart from mutations in the tumor suppressor gene NF2. Alternative tumorigenic mechanisms have been proposed, including a recurrent in-frame fusion transcript of the HTRA1 a...

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Detalles Bibliográficos
Autores principales: Taule-Sivertsen, Peter, Bruland, Ove, Håvik, Aril Løge, Bratland, Eirik, Lund-Johansen, Morten, Knappskog, Per Morten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Laboratory Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367919/
https://www.ncbi.nlm.nih.gov/pubmed/34213706
http://dx.doi.org/10.1007/s11060-021-03796-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367919/
https://www.ncbi.nlm.nih.gov/pubmed/34213706
http://dx.doi.org/10.1007/s11060-021-03796-6

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