1. Dastidar, Sumitava, Majumdar, Debanjana, Tipanee, Jaitip, Chuah, Marinee K, VandenDriessche, Thierry. 2021. Comprehensive transcriptome-wide analysis of spliceopathy correction of myotonic dystrophy using CRISPR-Cas9 in iPSCs-derived cardiomyocytes. In Molecular therapy : the journal of the American Society of Gene Therapy, 30, 75-91. doi:10.1016/j.ymthe.2021.08.004. https://pubmed.ncbi.nlm.nih.gov/34371182/
2. Matsson, Hans, Huss, Mikael, Persson, Helena, Peyrard-Janvid, Myriam, Kere, Juha. 2015. Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. In Journal of human genetics, 60, 399-401. doi:10.1038/jhg.2015.37. https://pubmed.ncbi.nlm.nih.gov/25877001/
3. Eicher, John D, Gruen, Jeffrey R. 2014. Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders. In Autism research : official journal of the International Society for Autism Research, 8, 229-34. doi:10.1002/aur.1436. https://pubmed.ncbi.nlm.nih.gov/25448322/
4. Melville, Scott A, Buros, Jacqueline, Parrado, Antonio R, Saykin, Andrew J, Farrer, Lindsay A. 2012. Multiple loci influencing hippocampal degeneration identified by genome scan. In Annals of neurology, 72, 65-75. doi:10.1002/ana.23644. https://pubmed.ncbi.nlm.nih.gov/22745009/
5. Shirasuna, K, Takeuchi, A, Bando, T, Nakajima, T, Oda, K. . The G10BP-1 gene encoding a GC box binding protein, is a target of Myc and Jun/Fos. In Genes to cells : devoted to molecular & cellular mechanisms, 4, 277-89. doi:. https://pubmed.ncbi.nlm.nih.gov/10421838/
6. Eden, S, Constancia, M, Hashimshony, T, Reik, W, Cedar, H. . An upstream repressor element plays a role in Igf2 imprinting. In The EMBO journal, 20, 3518-25. doi:. https://pubmed.ncbi.nlm.nih.gov/11432838/
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