Next-generation sequencing in the clinical genetic screening of patients with pheochromocytoma and paraganglioma

BACKGROUND: Recent findings have shown that up to 60% of pheochromocytomas (PCCs) and paragangliomas (PGLs) are caused by germline or somatic mutations in one of the 11 hitherto known susceptibility genes: SDHA, SDHB, SDHC, SDHD, SDHAF2, VHL, HIF2A (EPAS1), RET, NF1, TMEM127 and MAX. This list of ge...

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Detalles Bibliográficos
Autores principales: Crona, Joakim, Verdugo, Alberto Delgado, Granberg, Dan, Welin, Staffan, Stålberg, Peter, Hellman, Per, Björklund, Peyman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioScientifica 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682230/
https://www.ncbi.nlm.nih.gov/pubmed/23781326
http://dx.doi.org/10.1530/EC-13-0009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682230/
https://www.ncbi.nlm.nih.gov/pubmed/23781326
http://dx.doi.org/10.1530/EC-13-0009

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