A Korean Family of Familial Medullary Thyroid Cancer with Cys618Ser RET Germline Mutation

Familial medullary thyroid carcinoma (FMTC) is caused by autosomal dominant gain-of-function mutations in the RET proto-oncogene. An identifiable RET mutation can be detected in about 85% of FMTC families. The majority of germline mutations in FMTC have been found in exons 10 and 11 of the RET proto...

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Bibliografiske detaljer
Main Authors: Jung, Jinhyang, Uchino, Shinya, Lee, Youngha, Park, Hoyong
Format: Artigo
Sprog:Inglês
Udgivet: The Korean Academy of Medical Sciences 2010
Fag:
Original Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2811288/
https://ncbi.nlm.nih.gov/pubmed/20119574
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2010.25.2.226
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