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De novo KCNA6 variants with attenuated KV 1.6 channel deactivation in patients with epilepsy

Vincenzo Salpietro et al.
HAL (France) · Papers · License: Open Access
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neurodevelopmental-disorderwhole-exome-sequencing
0, Voltage-gated potassium channels, KV1 Shaker channel family, Whole exome sequencing, Neurodevelopmental disorder
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Record · ID 284382
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