Katavić, Matej, Monika Kukuruzović, Maša Malenica, Sara Seneca, and Ljerka Cvitanović-Šojat. “Distinctive Phenotype in a Girl With Rett Syndrome and a Novel 25 Bp Deletion Mutation in Exon 4 (c.881_905del25, nm_004992.3) of the MECP2 Gene”. Paediatria Croatica 58, no. 4 (December 30, 2014): 283–285. Accessed December 15, 2025. https://paedcro.izahost.com/index.php/paedcro/article/view/599.