Late-Onset Medullary Thyroid Cancer in a Patient with a Germline <i>RET</i> Codon C634R Mutation
<b>Background</b>: Multiple endocrine neoplasia type 2A (MEN2A) is a rare, hereditary syndrome resulting from a germline mutation in the <i>RET</i> proto-oncogene and characterized primarily by medullary thyroid cancer (MTC), pheochromocytoma (PHEO), and hyperparathyroidism. Types of <i>RET</i> muta...
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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI AG
2021-08-01
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| Colección: | Diagnostics |
| Materias: | |
| Acceso en línea: | https://www.mdpi.com/2075-4418/11/8/1448 |
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