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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Detalles Bibliográficos
Autores principales: Jung, Jinhyang, Uchino, Shinya, Lee, Youngha, Park, Hoyong
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2010
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811288/
https://www.ncbi.nlm.nih.gov/pubmed/20119574
http://dx.doi.org/10.3346/jkms.2010.25.2.226

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811288/
https://www.ncbi.nlm.nih.gov/pubmed/20119574
http://dx.doi.org/10.3346/jkms.2010.25.2.226

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