Multiple endocrine neoplasia type 1 variants and phenocopies
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary disease due to a mutation in the MEN1 tumor suppressor gene. The risk of the disease in first-degree relatives of MEN1 mutation carriers is 50%. MEN1 gene mutations are not identified in 10-30% of familiar MEN1 patien...
| Main Authors: | , , , , , |
|---|---|
| 格式: | 文件 |
| 语言: | Russian |
| 出版: |
"Consilium Medicum" Publishing house
2014-10-01
|
| 丛编: | Терапевтический архив |
| 主题: | |
| 在线阅读: | https://ter-arkhiv.ru/0040-3660/article/view/31611 |