The clinical genetics of phaeochromocytoma and paraganglioma
ABSTRACT 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 Neurofibromato...
| Hlavní autoři: | , |
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| Médium: | Článek |
| Jazyk: | English |
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Brazilian Society of Endocrinology and Metabolism
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| Edice: | Archives of Endocrinology and Metabolism |
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| On-line přístup: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972017000500490&lng=en&tlng=en |