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HARVARD Citation
Nakajima, J. et al. (n.d.). De novo EEF1A2 mutations in patients with characteristic facial features, intellectual disability, autistic behaviors and epilepsy. Clinical genetics. pp. 356-361. [Online].
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Nakajima, J. et al. (n.d.). De novo EEF1A2 mutations in patients with characteristic facial features, intellectual disability, autistic behaviors and epilepsy. Clinical genetics. pp. 356-361. [Online].