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Germline MEN1 mutations in sixteen Japanese families with multiple endocrine neoplasia type 1 (MEN1)
1999
European Journal of Endocrinology
Objective: Multiple endocrine neoplasia type 1 (MEN1) is a syndrome of endocrine tumors involving the parathyroids, anterior pituitary and enteropancreatic neuroendocrine tissues, and is inherited in an autosomal dominant manner. Recently, the gene responsible for this syndrome, MEN1, was positionally cloned in 11q13. We aimed to assess the significance of MEN1 gene diagnostics in families with MEN1. Design: Sixteen probands of familial MEN1 and their 40 family members were subjected to the
doi:10.1530/eje.0.1410475
pmid:10576763
fatcat:bfdta4gt45ez7l5ao44mkqym6u