Katavić, M., Kukuruzović, M., Malenica, M., Seneca, S., & Cvitanović-Šojat, L. (2014). 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(4), 283-285. https://doi.org/10.13112/PC.2014.49