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HARVARD Citation
Fazeli, W. (n.d.). FV 20 Dominant SCN2A mutation causes familial episodic ataxia and impairment of speech development. Clinical neurophysiology. 130 (8), pp. e131-e132. [Online].
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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), pp. e131-e132. [Online].