Browsing Psychiatry by Subject "MECP2 gene; Neurodevelopmental disorder; Rett syndrome"
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Rett syndrome in Ireland: a demographic study.
(2024)Background: Rett syndrome (RTT) is a rare neurodevelopmental condition associated with mutations in the gene coding for the methyl-CpG-binding protein 2 (MECP2). It is primarily observed in girls and affects individuals ...