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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...
保存先:
| 出版年: | BMC Med Genet |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2018
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| 主題: | |
| オンライン･アクセス: | 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 |
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