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Expression and functional analysis of menin in a multiple endocrine neoplasia type 1 (MEN1) patient with somatic loss of heterozygosity in chromosome 11q13 and unidentified germline mutation of theMEN1gene

✍ Scribed by Junko Naito; Hiroshi Kaji; Hideaki Sowa; Riko Kitazawa; Sohei Kitazawa; Toshihiko Tsukada; Geoffrey N. Hendy; Toshitsugu Sugimoto; Kazuo Chihara

Book ID: 111638237
Publisher: Springer
Year: 2006
Tongue: English
Weight: 729 KB
Volume: 29
Category: Article
ISSN: 0969-711X
DOI: 10.1385/endo:29:3:485

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Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by tumors in parathyroids, enteropancreatic endocrine tissues, anterior pituitary, and other tissues. The gene for MEN1 has recently been cloned and shown to code for a 610-amino acid protein of enigmatic func