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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Thyroid
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Mary Ann Liebert, Inc. 2016
Aiheet:
Thyroid Cancer and Nodules
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia