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Nathan Routledge

1PUBLICATIONS

1CO-AUTHORS

Neurology and neuromuscular diseases

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|Aug 29, 2025

Biallelic Truncating Variants in SCN3B Encoding Nav Channel Subunit β3 Lead to Neurodevelopmental Phenotype with and without Epilepsy and Ataxia.

Nathan Routledge, Maxime Lammens, Reza Maroofian

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Stephanie Efthymiou

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Stephanie Efthymiou

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