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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Detalhes bibliográficos
Publicado no:Thyroid
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2016
Assuntos:
Thyroid Cancer and Nodules
Acesso em linha: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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