Article
Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1: Additional information for mutational screening.
Human mutation - 1 Mar 2001
Asteria C, Faglia G, Roncoroni R, Borretta G, Ribotto P, Beck-Peccoz P
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