Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome.
Rett syndrome (RTT) is a severe neurodevelopmental disorder that affects about 1 in 10,000 female live births. The underlying cause of RTT is mutations in the X-linked gene, methyl-CpG-binding protein 2 (
Published In/Presented At
Osenberg, S., Karten, A., Sun, J., Li, J., Charkowick, S., Felice, C. A., Kritzer, M., Nguyen, M. V. C., Yu, P., & Ballas, N. (2018). Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome. Proceedings of the National Academy of Sciences of the United States of America, 115(23), E5363–E5372. https://doi.org/10.1073/pnas.1722546115
Medical Education | Medicine and Health Sciences
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