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Mutations in ASH1L disrupt the expression of the NTRK2 gene that encodes the TrkB receptor, leading to impaired neurite outgrowth and synaptic deficits associated with ASD [149]

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10.1038/srep01500 187 van TellingenO.Yetkin-ArikB.de GooijerM

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As a Nurse Practitioner specializing in medical aesthetics and regenerative medicine, I've seen firsthand how this peptide is quietly becoming one of the most talked-about recovery tools in functional medicine and for good reason