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MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism.
Grolmusz VK, Borka K, Kövesdi A, Németh K, Balogh K, Dékány C, Kiss A, Szentpéteri A, Sármán B, Somogyi A, Csajbók É, Valkusz Z, Tóth M, Igaz P, Rácz K, Patócs A. Grolmusz VK, et al. Among authors: dekany c. Virchows Arch. 2017 Sep;471(3):401-411. doi: 10.1007/s00428-017-2158-3. Epub 2017 Jun 8. Virchows Arch. 2017. PMID: 28597079