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] Filters: Author is Lara-Herguedas, Julián and Keyword is Exons [Clear All Filters]
De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects. Am J Med Genet A. 2021;185(3):877-883. doi:10.1002/ajmg.a.62017.