Whole-exome sequencing in children with dyslexia identifies rare variants in CLDN3 and ion channel genes (2024)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/2024.12.19.24319320
Publication URI: http://dx.doi.org/10.1101/2024.12.19.24319320
Type: Preprint