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HARVARD Citation
Strehlow, V. et al. (2022). Compound‐heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy. Epilepsia. 63 (10), pp. e132-e137. [Online].
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Strehlow, V. et al. (2022). Compound‐heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy. Epilepsia. 63 (10), pp. e132-e137. [Online].