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Fazeli, W. (n.d.). fV 20 Dominant SCN2A mutation causes familial episodic ataxia and impairment of speech development. Clinical neurophysiology, 130(8), e131–e132. http://access.bl.uk/ark:/81055/vdc_100086839187.0x000010
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Fazeli, W. (n.d.). fV 20 Dominant SCN2A mutation causes familial episodic ataxia and impairment of speech development. Clinical neurophysiology, 130(8), e131–e132. http://access.bl.uk/ark:/81055/vdc_100086839187.0x000010