Article
Review: multiple endocrine neoplasia type 1, sporadic neuroendocrine tumors, and MENIN.
Diagnostic molecular pathology : the American journal of surgical pathology, part B - 1 Sept 1999
Komminoth P
Abstract excerpt
Since the identification and cloning of the gene responsible for the inherited syndrome multiple endocrine neoplasia type 1 (MEN1) in 1997, important advances in the understanding of the disease, the encoded protein (MENIN) and its role in the development of sporadic neuroendocrine and other neoplasms have been made. In this review, the most important recently published data on the pathology of the MEN1 syndrome,...
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