A Clinicopathologic and Molecular Analysis of Fumarate Hydratase–deficient Pheochromocytoma and Paraganglioma

Up to 40% of pheochromocytomas (PCCs) and paragangliomas (PGLs) are hereditary. Germline mutations/deletions in fumarate hydratase (FH) cause hereditary leiomyomatosis and renal cell carcinoma syndrome which manifests predominantly with FH-deficient uterine/cutaneous leiomyomas and renal cell carcin...

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Detalles Bibliográficos
Autores principales: Fuchs, Talia L., Luxford, Catherine, Clarkson, Adele, Sheen, Amy, Sioson, Loretta, Elston, Marianne, Croxson, Michael S., Dwight, Trisha, Benn, Diana E., Tacon, Lyndal, Field, Michael, Ahadi, Mahsa S., Chou, Angela, Clifton-Bligh, Roderick J., Gill, Anthony J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760464/
https://www.ncbi.nlm.nih.gov/pubmed/35993574
http://dx.doi.org/10.1097/PAS.0000000000001945

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9760464/
https://www.ncbi.nlm.nih.gov/pubmed/35993574
http://dx.doi.org/10.1097/PAS.0000000000001945

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