Correlation between clinical features and MECP2 gene mutations in patients with Rett syndrome

Background: Rett syndrome is a progressive neurodevelopment disorder which mainly affects females and is a common cause of mental retardation. Loss of purposeful hand movements, regression of acquired cognitive and motor skills and autistic features are the main criteria associated with this disorde...

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Главные авторы: Hisham Megahed (Автор), Amina Hindawy (Автор), Mohamed Mohamady (Автор)
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Опубликовано: SpringerOpen, 2015-03-01T00:00:00Z.
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