Neurofibromatosis type 1 syndrome associated with gastrointestinal stromal tumor
Neurofibromatosis type 1 - NF1 (Recklinghausen's disease) is one of the most common hereditary tumor syndromes. The disease is caused by mutations in the NF1 gene, which is the tumor suppressor gene and the outcome of these mutations is the rapid uncontrolled growth of cells, as well as the hig...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
IP Habib O.N.
2015-06-01
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| Series: | Современная онкология |
| Subjects: | |
| Online Access: | https://modernonco.orscience.ru/1815-1434/article/view/26998 |