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Genetic mutations in P-Rex1 , a gene involved in regulating AMPAR endocytosis, have been identified in individuals with autism, and preclinical models lacking this gene exhibit behavioral phenotypes consistent with core features of ASD, including social deficits and reduced behavioral flexibility (Li et al., 2015)

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Practices routinely miscalculate annual frequency limits, omit required imaging documentation, or select the wrong code when the approach is transforaminal rather than interlaminar

Generally, a peptide comprises a minimum of two amino acids