Zobrazeno 1 - 1
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pro vyhledávání: '"Houda Ben Othmen"'
Autor:
Rania Ghorbel, Nourhene Fendri-Kriaa, Afif Ben Mahmoud, Marwa Kharrat, Ines Hsairi, Houda Kenoun, Houda Ben Othmen, Imen Abid, Chahnez Triki, Faiza Fakhfakh
Publikováno v:
Journal of Child Neurology. 30:1715-1721
Rett syndrome is a monogenic X-linked dominant neurodevelopmental disorder related to mutation in MECP2, which encodes the methyl-CpG–binding protein MeCP2. The aim of this study was to search for mutations of MECP2 gene in Tunisian Rett patients a