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[1] H. Vanbokhoven, G. Melino, E. Candi, W. Declercq, p63, a story of mice and men, J. Invest. Dermatol. 131 (2011) 1196–1207. [2] J. Celli, P. Duijf, B.C. Hamel, M. Bamshad, B. Kramer, A.P. Smits, et al., Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome, Cell 99 (1999) 143–153. [3] J. Schultz, C.P. Ponting, K. Hofmann, P. Bork, SAM as a protein interaction domain involved in developmental regulation, Protein Sci. 6 (1997) 249–253. [4] T. Goldsmith, O. Eytan, L. Magal, M. Solomon, S. Israeli, E. Warshauer, et al., A mutation in TP63 causing a mild ectodermal dysplasia phenotype, J. Invest. Dermatol. 134 (2014) 2277–2280. [5] D.O. Cicero, M. Falconi, E. Candi, S. Mele, B. Cadot, A. Di Venere, et al., NMR structure of the p63 SAM domain and dynamical properties of G534 V and T537P pathological mutants, identified in the AEC syndrome, Cell Biochem. Biophys. 44 (2006) 475–489. [6] A. Sathyamurthy, S.M. Freund, C.M. Johnson, M.D. Allen, M. Bycroft, Structural basis of p63a SAM domain mutants involved in AEC syndrome, FEBS J. 278 (2011) 2680–2688. [7] Y. Shimomura, M. Wajid, L. Shapiro, A.M. Christiano, P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle, Development 135 (2008) 743–753. [8] T. Rinne, E. Bolat, R. Meijer, H. Scheffer, H. van Bokhoven, Spectrum of p63 mutations in a selected patient cohort affected with ankyloblepharonectodermal defects-cleft lip/palate syndrome (AEC), Am. J. Med. Genet. 149 (2009) 1948–1951.