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

Silvia Paracchini (Creator)

Dataset

Date made available	2024
Publisher	GitHub

Software

Software

Contact

[email protected]

Access Dataset

https://github.com/kmarianski/DyslexiaWES_CLDN3

1 Finished

A genetic and functional genomic study: A genetic and functional genomic study of neurodevelopmental disorders
Paracchini, S. (PI)
The Royal Society
1/10/11 → 30/09/16
Project: Fellowship

1 Preprint

Whole-exome sequencing in children with dyslexia identifies rare variants in CLDN3 and ion channel genes
Marianski, K., Talcott, J. B., Stein, J., Monaco, A. P., Fisher, S. E., Bishop, D. V. M., Newbury, D. F. & Paracchini, S., 20 Dec 2024, medRxiv, 23 p.
Research output: Working paper › Preprint

Open Access

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