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HARVARD Citation
Zaha, K. et al. (2016). DNM1L‐related encephalopathy in infancy with Leigh syndrome‐like phenotype and suppression‐burst. Clinical genetics. 90 (5), pp. 472-474. [Online].
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Zaha, K. et al. (2016). DNM1L‐related encephalopathy in infancy with Leigh syndrome‐like phenotype and suppression‐burst. Clinical genetics. 90 (5), pp. 472-474. [Online].