KATAVIĆ, Matej; KUKURUZOVIĆ, Monika; MALENICA, Maša; SENECA, Sara; CVITANOVIĆ-ŠOJAT, Ljerka. 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, [S. l.], v. 58, n. 4, p. 283–285, 2014. DOI: 10.13112/PC.2014.49. Disponível em: https://paedcro.izahost.com/index.php/paedcro/article/view/599. Acesso em: 15 dec. 2025.