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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Bibliografiske detaljer
Udgivet i: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.
Format: Artigo
Sprog:Inglês
Udgivet: Mary Ann Liebert, Inc. 2016
Fag:
Thyroid Cancer and Nodules
Online adgang: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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