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Germline variant in REXO2 is a novel candidate gene in familial pheochromocytoma
Pheochromocytoma (PCC) is a rare, mostly benign tumour of the adrenal medulla. Hereditary PCC accounts for ~35% of cases and has been associated with germline mutations in several cancer susceptibility genes (e.g., KIF1B, SDHB, VHL, SDHD, RET). We performed whole-exome sequencing in a family with fo...
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| Pubblicato in: | Genet Res (Camb) |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Cambridge University Press
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7214532/ https://ncbi.nlm.nih.gov/pubmed/32354376 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0016672320000038 |
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