Whole-exome sequencing in children with dyslexia identifies rare variants in CLDN3 and ion channel genes (code)

Research output

Research output per year 2024 2024 2024

• 1 Article

Research output per year

Research output per year

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• 2024

  Whole-exome sequencing in children with dyslexia identifies rare variants in CLDN3 and ion channel genes

  Paracchini, S., 2024, In: medRxiv.

  Research output: Contribution to journal › Article