تحميل...
Loss of CDKL5 disrupts kinome profile and event-related potentials leading to autistic-like phenotypes in mice
Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene have been identified in neurodevelopmental disorders including atypical Rett syndrome (RTT), autism spectrum disorders (ASDs), and early infantile epileptic encephalopathy. The biological function of CDKL5 and its role in the etio...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , , , , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
National Academy of Sciences
2012
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| الموضوعات: | |
| الوصول للمادة أونلاين: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3535652/ https://ncbi.nlm.nih.gov/pubmed/23236174 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1216988110 |
| الوسوم: |
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