Insights into Mechanisms of Pheochromocytomas and Paragangliomas Driven by Known or New Genetic Drivers

SIMPLE SUMMARY: Pheochromocytomas and paragangliomas are rare neuroendocrine tumors that are often hereditary. Although research has advanced considerably, significant gaps still persist in understanding risk factors, predicting metastatic potential and treating aggressive tumors. The study of rare...

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Detalles Bibliográficos
Autores principales: Flores, Shahida K., Estrada-Zuniga, Cynthia M., Thallapureddy, Keerthi, Armaiz-Peña, Gustavo, Dahia, Patricia L. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467373/
https://www.ncbi.nlm.nih.gov/pubmed/34572828
http://dx.doi.org/10.3390/cancers13184602

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467373/
https://www.ncbi.nlm.nih.gov/pubmed/34572828
http://dx.doi.org/10.3390/cancers13184602

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