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HARVARD Citation
Smigiel, R. et al. (2016). Further evidence for GRIN2B mutation as the cause of severe epileptic encephalopathy. American journal of medical genetics. 170 (12), pp. 3265-3270. [Online].
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Smigiel, R. et al. (2016). Further evidence for GRIN2B mutation as the cause of severe epileptic encephalopathy. American journal of medical genetics. 170 (12), pp. 3265-3270. [Online].