Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome

Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome

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...

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Bibliographic Details
Main Authors: Huong Le Thi Thanh, Trinh Do Thi Diem, Chinh Vu Duy, Ha Ly Thi Thanh, Hoa Bui Thi Phuong, Liem Nguyen Thanh
Format: Article
Language:English
Published: BMC 2018-08-01
Series:BMC Medical Genetics
Subjects:
RETT syndrome
Neurodevelopmental disorder
MECP2
Mutation spectrum
de novo
Novel mutation
Online Access:http://link.springer.com/article/10.1186/s12881-018-0658-x

Internet

http://link.springer.com/article/10.1186/s12881-018-0658-x

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