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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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Bibliografski detalji
Izdano u:Jpn J Cancer Res
Glavni autori: Takano, Torn, Miyauchi, Akira, Yoshida, Hiroshi, Hasegawa, Yukiko, Kuma, Kanji, Amino, Nobuyuki
Format: Artigo
Jezik:Inglês
Izdano: Blackwell Publishing Ltd 2001
Teme:
Online pristup: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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