Large‐scale Analysis of Mutations in RET Exon 16 in Sporadic Medullary Thyroid Carcinomas in Japan

Germline mutations in the RET proto‐oncogene are the cause of multiple endocrine neoplasia type 2 (MEN 2A and 2B) and familial medullary thyroid carcinoma (FMTC). Some cases of sporadic medullary thyroid carcinoma (MTC) have also been reported to have mutations in the RET gene. However, two previous...

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Detalles Bibliográficos
Autores principales: Takano, Torn, Miyauchi, Akira, Yoshida, Hiroshi, Hasegawa, Yukiko, Kuma, Kanji, Amino, Nobuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2001
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926749/
https://www.ncbi.nlm.nih.gov/pubmed/11429053
http://dx.doi.org/10.1111/j.1349-7006.2001.tb01143.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926749/
https://www.ncbi.nlm.nih.gov/pubmed/11429053
http://dx.doi.org/10.1111/j.1349-7006.2001.tb01143.x

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