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HARVARD Citation
Akamine, S. et al. (2018). Early‐onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2. Epilepsia open. 3 (1), pp. 81-85. [Online].
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Akamine, S. et al. (2018). Early‐onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2. Epilepsia open. 3 (1), pp. 81-85. [Online].