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

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Published inPaediatria Croatica Vol. 58; no. 4; pp. 283 - 5
Main Authors Katavić, Matej, Kukuruzović, Monika, Malenica, Maša, Seneca, Saša, Cvitanović Šojat, Ljerka
Format Journal Article
LanguageEnglish
Published 30.12.2014
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ISSN:1330-1403
DOI:10.13112/PC.2014.49