Two Germline Missense Mutations at Codons 804 and 806 of the RET Proto‐oncogene in the Same Allele in a Patient with Multiple Endocrine Neoplasia Type 2B without Codon 918 Mutation

Multiple endocrine neoplasia (MEN) type 2B is a clinically distinct entity among the autosomal dominant MEN 2 syndromes. Most patients with MEN 2B carry a germline mutation (M918T) of the RET proto‐oncogene, while a few carry A883F. We examined a patient with MEN 2B, but without M918T or A883F, and...

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Detalhes bibliográficos
Publicado no:Jpn J Cancer Res
Main Authors: Miyauchi, Akira, Futami, Hitoyasu, Hai, Noritaka, Yokozawa, Tamotsu, Kuma, Kanji, Aoki, Norihiko, Kosugi, Shinji, Sugano, Kokichi, Yamaguchi, Ken
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Publishing Ltd 1999
Assuntos:
Rapid Communication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5925979/
https://ncbi.nlm.nih.gov/pubmed/10076558
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1349-7006.1999.tb00658.x
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