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19,27,28 In addition, rare copy number variants are also identified to be related to MDD risk, there may be three copy number variants (CNV) loci associated with Prader-Willis syndrome: 1q21.1 duplication, 15q11-13, and 16p11.2

However, we also covered the importance of understanding that while the benefits can be profound for some, large-scale scientific studies are still ongoing to fully validate all its widespread claims

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