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...

詳細記述

保存先:
書誌詳細
出版年:Thyroid
主要な著者: Xu, Jian Yu, Grubbs, Elizabeth G., Waguespack, Steven G., Jimenez, Camilo, Gagel, Robert F., Sosa, Julie A., Sellin, Rena V., Dadu, Ramona, Hu, Mimi I., Trotter, Chardria S., Jackson, Michelle, Rich, Thereasa A., Hyde, Samuel M., Sherman, Steven I., Cote, Gilbert J.
フォーマット: Artigo
言語:Inglês
出版事項: Mary Ann Liebert, Inc. 2016
主題:
Thyroid Cancer and Nodules
オンライン･アクセス: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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