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HARVARD Citation
Fry, A. et al. (2016). Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. BMC medical genetics. 17 (1), pp. 1-9. [Online].
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Fry, A. et al. (2016). Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. BMC medical genetics. 17 (1), pp. 1-9. [Online].