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The use genetic models is rooted in the substantial heritability of the ASD with at least 20% of individuals diagnosed with ASD have underlying genetic causes in de novo mutations, copy number variations, point mutations, and chromosomal changes [14]

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In this review, the clinical sign and symptoms were reviewed and optimal treatments were suggested

This may be attributed to the very low clearance rate in the ICRP model for lower respiratory tract clearance or to the sensitive transcriptomics PoDs