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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Vydáno v:Oncotarget
Hlavní autoři: Albattal, Shatha, Alswailem, Meshael, Moria, Yosra, Al-Hindi, Hindi, Dasouki, Majed, Abouelhoda, Mohamed, Alkhail, Hala Aba, Alsuhaibani, Entissar, Alzahrani, Ali S.
Médium: Artigo
Jazyk:Inglês
Vydáno: Impact Journals LLC 2019
Témata:
Research Paper
On-line přístup: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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