Llwytho...
Investigation of Rett Syndrome using pluripotent stem cells
Rett Syndrome (RTT) is one of most prevalent female neurodevelopmental disorders. De novo mutations in X-linked MECP2 are mostly responsible for RTT. Since the identification of MeCP2 as the underlying cause of RTT, murine models have contributed to understanding the pathophysiology of RTT and funct...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2013
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3773984/ https://ncbi.nlm.nih.gov/pubmed/23744605 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcb.24597 |
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