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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Detalhes bibliográficos
Main Authors: Crona, Joakim, Nordling, Margareta, Maharjan, Rajani, Granberg, Dan, Stålberg, Peter, Hellman, Per, Björklund, Peyman
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3899286/
https://ncbi.nlm.nih.gov/pubmed/24466223
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0086756
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