Caracterização molecular de uma família com nem2a e suas implicações clínicas.
MEN2A is an autossomal dominant cancer syndrome characterised by the presence of medullary thyroid cancer, pheochromocytoma and primary hyperparathyroidism. Germline mutations of the RET protooncogene constitute the molecular defect and can be identified in affected individuals. Genetic screening of...
| Published in: | Acta Médica Portuguesa |
|---|---|
| Main Authors: | , , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Ordem dos Médicos
2003-08-01
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| Online Access: | https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1188 |