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Clinical phenotype and genetic features of 16p11.2 microdeletion-related epilepsy in children http://www.zgddek.com/EN/10.7499/j.issn.1008-8830.2111110
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Clinical phenotype and genetic features of 16p11.2 microdeletion-related epilepsy in children http://www.zgddek.com/EN/10.7499/j.issn.1008-8830.2111110
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