Loading...
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...
Na minha lista:
| Udgivet i: | BMC Med Genet |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2018
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6090653/ https://ncbi.nlm.nih.gov/pubmed/30081849 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0658-x |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|