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

Silvia Paracchini

Research output: Contribution to journal › Article

Original language	English
Journal	medRxiv
Publication status	Published - 2024

Access to Document

https://www.medrxiv.org/content/10.1101/2024.12.19.24319320v1Licence: CC BY

Whole-exome sequencing in children with dyslexia identifies rare variants in CLDN3 and ion channel genes (code)
Paracchini, S. (Creator), GitHub, 2024
https://github.com/kmarianski/DyslexiaWES_CLDN3
Dataset: Software

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