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Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome
New research suggests that common pathways are altered in many neurodevelopmental disorders including autism spectrum disorder; however, little is known about early molecular events that contribute to the pathology of these diseases. The study of monogenic, neurodevelopmental disorders with a high i...
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| 出版年: | Brain |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5837342/ https://ncbi.nlm.nih.gov/pubmed/28137726 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/aww357 |
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