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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...
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| Publicado no: | Oncotarget |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Impact Journals LLC
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6800268/ https://ncbi.nlm.nih.gov/pubmed/31666924 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.27194 |
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