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Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis
Multiple endocrine neoplasia type 2 (MEN 2) is an inherited cancer syndrome characterised by medullary thyroid carcinoma (MTC), with or without phaeochromocytoma and hyperparathyroidism. MEN 2 is unusual among cancer syndromes as it is caused by activation of a cellular oncogene, RET. Germline mutat...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMJ Group
2000
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1734482/ https://ncbi.nlm.nih.gov/pubmed/11073534 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.37.11.817 |
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