Analysis of MEN1 c.482GA mutation in a pedigree with familial multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the development of neuroendocrine tumors, which in turn are caused by mutations in the MEN1 gene. In the present study, a case of a 46-year-old woman who was clinically diagnosed with MEN1 based on the pres...

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Veröffentlicht in:	Molecular medicine reports 2017-12, Vol.16 (6), p.8973
Hauptverfasser:	Luo, Yuanyuan, Sun, Yongxiang, Zhu, Xiaofan, Li, Xialian
Format:	Artikel
Sprache:	eng
Schlagworte:	Analysis Causes of Diagnosis Gene mutation Genetic aspects Genetic research Genetic testing Health aspects Neuroendocrine tumors Prolactin
Online-Zugang:	Volltext
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