새로운 MEN1 유전자 돌연변이가 증명된 위, 십이지장, 췌장의 신경내분비종양

Multiple endocrine neoplasia type 1 (MEN1) syndrome is a relatively rare disease, characterized by the occurrence of multiple endocrine tumors in the parathyroid and pituitary glands as well as the pancreas. Here, we report a case of MEN1 with neuroendocrine tumors (NETs) in the stomach, duodenum, a...

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Veröffentlicht in:	The Korean journal of gastroenterology 2017-03, Vol.69 (3), p.181
Hauptverfasser:	양민아, Min A Yang, 이웅기, Woong Ki Lee, 신홍식, Hong Shik Shin, 박성현, Sung Hyun Park, 김병선, Byung Sun Kim, 김지웅, Ji Woong Kim, 조진웅, Jin Woong Cho, 윤소희, So Hee Yun
Format:	Artikel
Sprache:	kor
Schlagworte:	Endoscopy Germ-line mutation INDEL mutation Multiple endocrine neoplasia type 1 Neuroendocrine tumors
Online-Zugang:	Volltext
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