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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Bibliografiska uppgifter
I publikationen:Thyroid
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Mary Ann Liebert, Inc. 2016
Ämnen:
Thyroid Cancer and Nodules
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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