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The clinical genetics of phaeochromocytoma and paraganglioma
Phaeochromocytoma and paraganglioma are rare catecholamine-producing tumours, recognised to have one of the richest hereditary backgrounds of all neoplasms, with germline mutations seen in approximately 30% of patients. They can be a part of genetic syndromes such as MEN 2 or Neurofibromatosis type...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Sociedade Brasileira de Endocrinologia e Metabologia
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522248/ https://www.ncbi.nlm.nih.gov/pubmed/29166454 http://dx.doi.org/10.1590/2359-3997000000299 |