MeCP2 in the regulation of neural activity: Rett syndrome pathophysiological perspectives

Rett syndrome (RTT), an X-linked neurodevelopment disorder, occurs in approximately one out of 10,000 females. Individuals afflicted by RTT display a constellation of signs and symptoms, affecting nearly every organ system. Most striking are the neurological manifestations, including regression of l...

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Veröffentlicht in:Degenerative Neurological and Neuromuscular Disease 2015-01, Vol.5, p.103-116
Hauptverfasser: Cuddapah, Vishnu Anand, Nwaobi, Sinifunanya Elvee, Percy, Alan K, Olsen, Michelle Lynne
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Sprache:eng
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