p.L105Vfs mutation in a family with thymic neuroendocrine tumor combined with MEN1: a case report

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder arising from mutations of the MEN1 tumor suppressor gene on chromosome 11q13; MEN1 is characterized by the development of neuroendocrine tumors, including those of the parathyroid, gastrointestinal endocrine...

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Detalles Bibliográficos
Autores principales: Zheng, Hongjuan, Zhou, Shishi, Tang, Wanfen, Wang, Qinghua, Zhang, Xia, Jin, Xiayun, Yuan, Ying, Fu, Jianfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055077/
https://www.ncbi.nlm.nih.gov/pubmed/32126984
http://dx.doi.org/10.1186/s12883-020-01659-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055077/
https://www.ncbi.nlm.nih.gov/pubmed/32126984
http://dx.doi.org/10.1186/s12883-020-01659-7

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