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Epilepsy and genetic in Rett syndrome: A review
INTRODUCTION: Rett syndrome (RTT) is a severe X‐linked neurodevelopmental disorder that primarily affects girls, with an incidence of 1:10,000–20,000. The diagnosis is based on clinical features: an initial period of apparently normal development (ages 6–12 months) followed by a rapid decline with r...
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| 出版年: | Brain Behav |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6520293/ https://ncbi.nlm.nih.gov/pubmed/30929312 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/brb3.1250 |
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