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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Bibliographic Details
Published in:Jpn J Cancer Res
Main Authors: Takano, Torn, Miyauchi, Akira, Yoshida, Hiroshi, Hasegawa, Yukiko, Kuma, Kanji, Amino, Nobuyuki
Format: Artigo
Language:Inglês
Published: Blackwell Publishing Ltd 2001
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Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5926749/
https://ncbi.nlm.nih.gov/pubmed/11429053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1349-7006.2001.tb01143.x
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