Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paraganglioma

About 30%–40% of patients with pheochromocytoma (PCC) and paraganglioma (PGL) have underlying germline mutations in certain susceptibility genes despite absent family history of these tumors. Here, we present mutational profile of 101 such patients with PCC/PGL (PPGL) from the highly consanguineous...

Descripción completa

Detalles Bibliográficos
Autores principales: Albattal, Shatha, Alswailem, Meshael, Moria, Yosra, Al-Hindi, Hindi, Dasouki, Majed, Abouelhoda, Mohamed, Alkhail, Hala Aba, Alsuhaibani, Entissar, Alzahrani, Ali S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800268/
https://www.ncbi.nlm.nih.gov/pubmed/31666924
http://dx.doi.org/10.18632/oncotarget.27194

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800268/
https://www.ncbi.nlm.nih.gov/pubmed/31666924
http://dx.doi.org/10.18632/oncotarget.27194

Ejemplares similares