Familial Clinical Heterogeneity of Medullary Thyroid Cancer with Germline RET S891A Protooncogene Mutation: 7-year Follow-up with Successful Sorafenib Treatment
Hereditary forms of medullary thyroid carcinoma (MTC) are rare. Different phenotypes with the same mutation may be due to differences in the timing of rearranged during transfection (RET) activation steps, additional mutations in other regions of the gene, or the co-occurrence of germline and somati...
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| Main Authors: | , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Galenos Yayincilik
2025-09-01
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| Series: | JCRPE |
| Subjects: | |
| Online Access: | https://www.jcrpe.org/articles/familial-clinical-heterogeneity-of-medullary-thyroid-cancer-with-germline-lessemgreaterretlessemgreater-s891a-protooncogene-mutation-7-year-follow-up-with-successful-sorafenib-treatment/doi/jcrpe.galenos.2023.2023-7-13 |
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