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Autor:
Hong Pan, Xi Ru Wu, Xinhua Bao, Laila Robertson, Mary Carey, Helen Leonard, Hannah C. Moore, Sarah L. Williamson, John Christodoulou, Sonj Hall, Sue Fyfe, Nicholas de Klerk
Publikováno v:
Brain and Development. 27:S59-S68
Background: Rett syndrome is a neurodevelopmental disorder mostly affecting females and caused by mutations in the MECP2 gene. Originally the syndrome was characterised as having a normal prenatal and perinatal period with later regression. Previous