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Whole-exome sequencing in children with dyslexia identifies rare variants in CLDN3 and ion channel genes
Marianski K., Talcott JB., Stein J., Monaco AP., Fisher SE., Bishop DVM., Newbury DF., Paracchini S.
DOI
10.1101/2024.12.19.24319320
Type
Preprint
Publication Date
2024-12-20T00:00:00+00:00