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publicationName Experimental Neurology
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bibliographicCitation Poliquin S, Hughes I, Shen W, Mermer F, Wang J, Mack T, Xu D, Kang J. Genetic mosaicism, intrafamilial phenotypic heterogeneity, and molecular defects of a novel missense SLC6A1 mutation associated with epilepsy and ADHD. Experimental Neurology. 2021 Aug;342():113723. doi: 10.1016/j.expneurol.2021.113723.
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date 202108
identifier https://pubmed.ncbi.nlm.nih.gov/PMC9116449
https://doi.org/10.1016/j.expneurol.2021.113723
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language English
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title Genetic mosaicism, intrafamilial phenotypic heterogeneity, and molecular defects of a novel missense SLC6A1 mutation associated with epilepsy and ADHD
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