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78,79 In addition, rare de novo mutations of CHD8, SCN1A, SCN2A, SYNGAP1, ARID1B, GRIN2B, DSCAM, TBR1, KATNAL2, LAMC3 and NTNG1 have been identified, with strong evidence for their association with ASD

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(5) Rajman L, et al

[1] This medication is available through both 503A compounding pharmacies and 503B outsourcing facilities, meaning it can be prepared for individual prescriptions or in bulk for office use