PTCH1 mutant small cell glioblastoma in a patient with Gorlin syndrome: A case report

Gorlin syndrome or nevoid basal cell carcinoma syndrome is a rare genetic disease characterized by predisposition to congenital defects, basal cell carcinomas and medulloblastoma. The syndrome results from a heritable mutation in PATCHED1 (PTCH1), causing constitutive activation of the Hedgehog path...

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Detalles Bibliográficos
Autores principales: Dorsey, John T., Mott, Ryan T., Lack, Christopher M., Britt, Nicholas, Ramkissoon, Shakti H., Morris, Bonny B., Carter, Annette, Detroye, Alisha T., Chan, Michael, Tatter, Stephen, Lesser, Glenn J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353864/
https://www.ncbi.nlm.nih.gov/pubmed/35949590
http://dx.doi.org/10.3892/ol.2022.13446

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353864/
https://www.ncbi.nlm.nih.gov/pubmed/35949590
http://dx.doi.org/10.3892/ol.2022.13446

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