Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Thyroid |
|---|---|
| Prif Awduron: | , , , , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Mary Ann Liebert, Inc.
2016
|
| Pynciau: | |
| Mynediad Ar-lein: | 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 |
| Tagiau: |
Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|