Investigating the role of somatic sequencing platforms for phaeochromocytoma and paraganglioma in a large UK cohort

OBJECTIVES: Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumours with malignant potential and a hereditary basis in almost 40% of patients. Germline genetic testing has transformed the management of PPGL enabling stratification of surveillance approaches, earlier diagnosis an...

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Detalles Bibliográficos
Autores principales: Winzeler, Bettina, Tufton, Nicola, S. Lim, Eugenie, Challis, Ben G., Park, Soo‐Mi, Izatt, Louise, Carroll, Paul V., Velusamy, Anand, Hulse, Tony, Whitelaw, Benjamin C., Martin, Ezequiel, Rodger, Fay, Maranian, Melanie, Clark, Graeme R., A. Akker, Scott, Maher, Eamonn R., Casey, Ruth T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Invited Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543043/
https://www.ncbi.nlm.nih.gov/pubmed/34870338
http://dx.doi.org/10.1111/cen.14639

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543043/
https://www.ncbi.nlm.nih.gov/pubmed/34870338
http://dx.doi.org/10.1111/cen.14639

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