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Medullary Thyroid Carcinoma Associated with Germline RET(K666N) Mutation
Background: Multiple endocrine neoplasia type 2 is an autosomal dominant inherited syndrome caused by activating mutations in the RET proto-oncogene. The RET(K666N) DNA variant was previously reported in two isolated medullary thyroid carcinoma (MTC) cases, but no family studies are available, and i...
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| I publikationen: | Thyroid |
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| Huvudupphovsmän: | , , , , , , , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Mary Ann Liebert, Inc.
2016
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5175438/ https://ncbi.nlm.nih.gov/pubmed/27673361 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/thy.2016.0374 |
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