Clinical features and signaling effects of RET D631Y variant multiple endocrine neoplasia type 2 (MEN2)

BACKGROUND/AIMS: Germline mutations of the rearranged during transfection (RET) gene cause multiple endocrine neoplasia type 2 (MEN2). About 85% of RET mutations in MEN2 occur in codon Cys634. The RET D631Y mutation has recently been discovered, and we have studied its molecular expression and clini...

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Detalles Bibliográficos
Autores principales: Lee, Ji-young, Kim, Su Yeon, Jo, Kwan Hoon, Mo, Eun Yeong, Kim, Eun Sook, Kim, Hye Soo, Han, Je Ho, Moon, Sung-dae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925960/
https://www.ncbi.nlm.nih.gov/pubmed/34905813
http://dx.doi.org/10.3904/kjim.2021.311

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925960/
https://www.ncbi.nlm.nih.gov/pubmed/34905813
http://dx.doi.org/10.3904/kjim.2021.311

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