Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families

BACKGROUD: Multiple endocrine neoplasia type 2A (MEN2A) is a condition with inherited autosomal dominant mutations in RET (rearranged during transfection) gene that predisposes the carrier to extremely high risk of medullary thyroid cancer (MTC) and other MEN2A-associated tumors such as parathyroid...

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Detalles Bibliográficos
Autores principales: Liu, Qiuli, Tong, Dali, Yuan, Wenqiang, Liu, Gaolei, Yuan, Gang, Lan, Weihua, Zhang, Dianzheng, Zhang, Jun, Huang, Zaoming, Zhang, Yao, Jiang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
4300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5279108/
https://www.ncbi.nlm.nih.gov/pubmed/28099363
http://dx.doi.org/10.1097/MD.0000000000005967

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5279108/
https://www.ncbi.nlm.nih.gov/pubmed/28099363
http://dx.doi.org/10.1097/MD.0000000000005967

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