Spectrum of MECP2 mutations in Vietnamese patients with RETT syndrome

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 mutation...

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Detalles Bibliográficos
Autores principales: Le Thi Thanh, Huong, Do Thi Diem, Trinh, Duy, Chinh Vu, Thanh, Ha Ly Thi, Phuong, Hoa Bui Thi, Thanh, Liem Nguyen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090653/
https://www.ncbi.nlm.nih.gov/pubmed/30081849
http://dx.doi.org/10.1186/s12881-018-0658-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090653/
https://www.ncbi.nlm.nih.gov/pubmed/30081849
http://dx.doi.org/10.1186/s12881-018-0658-x

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