Model systems in SDHx-related pheochromocytoma/paraganglioma

Pheochromocytoma (PHEO) and paraganglioma (PGL) (together PPGL) are tumors with poor outcomes that arise from neuroendocrine cells in the adrenal gland, and sympathetic and parasympathetic ganglia outside the adrenal gland, respectively. Many follow germline mutations in genes coding for subunits of...

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Detalles Bibliográficos
Autores principales: Takács-Vellai, Krisztina, Farkas, Zsolt, Ősz, Fanni, Stewart, Gordon W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825606/
https://www.ncbi.nlm.nih.gov/pubmed/34957538
http://dx.doi.org/10.1007/s10555-021-10009-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825606/
https://www.ncbi.nlm.nih.gov/pubmed/34957538
http://dx.doi.org/10.1007/s10555-021-10009-z

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