Integrative Genetic Characterization and Phenotype Correlations in Pheochromocytoma and Paraganglioma Tumours

BACKGROUND: About 60% of Pheochromocytoma (PCC) and Paraganglioma (PGL) patients have either germline or somatic mutations in one of the 12 proposed disease causing genes; SDHA, SDHB, SDHC, SDHD, SDHAF2, VHL, EPAS1, RET, NF1, TMEM127, MAX and H-RAS. Selective screening for germline mutations is rout...

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Detalles Bibliográficos
Autores principales: Crona, Joakim, Nordling, Margareta, Maharjan, Rajani, Granberg, Dan, Stålberg, Peter, Hellman, Per, Björklund, Peyman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899286/
https://www.ncbi.nlm.nih.gov/pubmed/24466223
http://dx.doi.org/10.1371/journal.pone.0086756

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899286/
https://www.ncbi.nlm.nih.gov/pubmed/24466223
http://dx.doi.org/10.1371/journal.pone.0086756

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