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Association of genetic variants, such as the μ-opioid receptor 1 (OPRM1) rs1799971 and catechol-O-methyltransferase (COMT) rs4680, with phenotypic expression of fibromyalgia62

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Association of genetic variants, such as the μ-opioid receptor 1 (OPRM1) rs1799971 and catechol-O-methyltransferase (COMT) rs4680, with phenotypic expression of fibromyalgia62

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