Genetic and Epigenetic Analysis in Korean Patients with Multiple Endocrine Neoplasia Type 1

Background: Multiple endocrine neoplasia type 1 (MEN1) is a familial syndrome characterized by the parathyroid, pancreas and pituitary tumors. Parathyroid tumors are the most common clinical manifestations, occurring in more than 90% of MEN1 patients. Heterozygous germline mutations of the MENIN gen...

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Veröffentlicht in:	Endocrinology and metabolism (Seoul) 2014-09, Vol.29 (3), p.270
Hauptverfasser:	Yoon Jung Chung, Sena Hwang, Jong Ju Jeong, Sun Yong Song, Se Hoon Kim, Yu Mie Rhee
Format:	Artikel
Sprache:	kor
Schlagworte:	DNA methylation Germ-line mutation Korea Multiple endocrine neoplasia type 1
Online-Zugang:	Volltext
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