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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Detalles Bibliográficos
Autores principales: Miyauchi, Akira, Futami, Hitoyasu, Hai, Noritaka, Yokozawa, Tamotsu, Kuma, Kanji, Aoki, Norihiko, Kosugi, Shinji, Sugano, Kokichi, Yamaguchi, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1999
Materias:
Rapid Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5925979/
https://www.ncbi.nlm.nih.gov/pubmed/10076558
http://dx.doi.org/10.1111/j.1349-7006.1999.tb00658.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5925979/
https://www.ncbi.nlm.nih.gov/pubmed/10076558
http://dx.doi.org/10.1111/j.1349-7006.1999.tb00658.x

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