Co-occurrence of mutations in NF1 and other susceptibility genes in pheochromocytoma and paraganglioma

INTRODUCTION: The percentage of patients diagnosed with pheochromocytoma and paraganglioma (altogether PPGL) carrying known germline mutations in one of the over fifteen susceptibility genes identified to date has dramatically increased during the last two decades, accounting for up to 35-40% of PPG...

Descripción completa

Detalles Bibliográficos
Autores principales: Mellid, Sara, Gil, Eduardo, Letón, Rocío, Caleiras, Eduardo, Honrado, Emiliano, Richter, Susan, Palacios, Nuria, Lahera, Marcos, Galofré, Juan C., López-Fernández, Adriá, Calatayud, Maria, Herrera-Martínez, Aura D., Galvez, María A., Matias-Guiu, Xavier, Balbín, Milagros, Korpershoek, Esther, Lim, Eugénie S., Maletta, Francesca, Lider, Sofia, Fliedner, Stephanie M. J., Bechmann, Nicole, Eisenhofer, Graeme, Canu, Letizia, Rapizzi, Elena, Bancos, Irina, Robledo, Mercedes, Cascón, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905101/
https://www.ncbi.nlm.nih.gov/pubmed/36760809
http://dx.doi.org/10.3389/fendo.2022.1070074

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905101/
https://www.ncbi.nlm.nih.gov/pubmed/36760809
http://dx.doi.org/10.3389/fendo.2022.1070074

Ejemplares similares