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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Detalles Bibliográficos
Autores principales: Laitman, Yael, Tzur, Shay, Attai, Ruben, Tirosh, Amit, Friedman, Eitan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2020
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214532/
https://www.ncbi.nlm.nih.gov/pubmed/32354376
http://dx.doi.org/10.1017/S0016672320000038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214532/
https://www.ncbi.nlm.nih.gov/pubmed/32354376
http://dx.doi.org/10.1017/S0016672320000038

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