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Next-generation sequencing for the diagnosis of hereditary pheochromocytoma and paraganglioma syndromes

PURPOSE OF REVIEW: About 40% of the neuroendocrine tumors pheochromocytomas and paragangliomas (PPGLs) are caused by an inherited mutation. Diagnostic genetic screening is recommended for patients and their families. However, the number of susceptibility genes involved is high and continues to grow,...

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Detalhes bibliográficos
Publicado no:Curr Opin Endocrinol Diabetes Obes
Main Authors: Toledo, Rodrigo A., Dahia, Patricia L.M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7216557/
https://ncbi.nlm.nih.gov/pubmed/25871962
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MED.0000000000000150
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