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  • Molecular assay reagents intended to identify mutations in the multiple endocrine neoplasia I (MEN1) gene, located at chromosome 11q13, which encodes for menin that acts as a tumor suppressor. Mutations at this locus have been identified in patients with multiple endocrine neoplasia type I, hyperparathyroidism, Wermer syndrome (MEN1 defect), and carcinoid tumors of the lungs.
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