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Update on Multiple Endocrine Neoplasia Type 2: Focus on Medullary Thyroid Carcinoma
Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant hereditary cancer syndrome caused by missense gain-of-function mutations in the RET proto-oncogene on chromosome 10. Specific RET mutations can predispose toward a particular phenotype and clinical course, with strong genotype–pheno...
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| Pubblicato in: | J Endocr Soc |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Endocrine Society
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6065486/ https://ncbi.nlm.nih.gov/pubmed/30087948 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2018-00178 |
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