Whole-exome sequencing of nearly 1000 individuals identified SCN2A as the sole gene in which two independent probands had non-sense variants that disrupted the same gene, a highly significant result [ 22 ].
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Whole-exome sequencing of nearly 1000 individuals identified SCN2A as the sole gene in which two independent probands had non-sense variants that disrupted the same gene, a highly significant result [ 22 ].