Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome

• Main Authors: Huong Le Thi Thanh (Author), Trinh Do Thi Diem (Author), Chinh Vu Duy (Author), Ha Ly Thi Thanh (Author), Hoa Bui Thi Phuong (Author), Liem Nguyen Thanh (Author)
• Format: Book
• Published: BMC, 2018-08-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Rett syndrome (RTT) is a severe neurodevelopmental disorder in children characterized by a normal neurodevelopmental process in the first 6-18 months followed by a period of motor and vocal deterioration with stereotypic hand movements. Incidence of RTT is mostly due to de novo m...