제1형 신경섬유종증 환자에서 발생한 대장암

Neurofibromatosis type I is an autosomal dominant disorder that occurs once in 3,000 births. It is characterized by neurofibromas and caf?au lait spots of the skin. Neurofibromatosis type I gene is a tumor suppressor gene. Patients with neurofibromatosis type I are at an increased risk of developing...

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Veröffentlicht in:	The Korean journal of gastroenterology 2002-12, Vol.40 (6), p.402
Hauptverfasser:	김광진, Kwang Jin Kim, 최석렬, Seok Reyol Choi, 손승현, Seung Hyun Sohn, 이상, Sang Lee, 홍기봉, Ki Bong Hong, 금동주, Dong Joo Keum, 지삼룡, Sam Ryong Jee, 이종훈, Jong Hoon Lee, 한상영, Sang Young Han, 신우원, Woo Won Shin
Format:	Artikel
Sprache:	kor
Schlagworte:	Colon neoplasms Neurofibromatosis I
Online-Zugang:	Volltext
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