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Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families
BACKGROUD: Multiple endocrine neoplasia type 2A (MEN2A) is a condition with inherited autosomal dominant mutations in RET (rearranged during transfection) gene that predisposes the carrier to extremely high risk of medullary thyroid cancer (MTC) and other MEN2A-associated tumors such as parathyroid...
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| Опубликовано в: : | Medicine (Baltimore) |
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| Главные авторы: | , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Wolters Kluwer Health
2017
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5279108/ https://ncbi.nlm.nih.gov/pubmed/28099363 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000005967 |
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