TY  - JOUR 
AU  - Gómez Castro, Julia
AU  - Estepa Hernández, Sandra
AU  - Chicharro Miguel, Celia
AU  - Peiró Cárdenas, Regina
AU  - Fernández-Araque, Ana
AU  - Verde, Zoraida
AU  - Erenas Ondategui, Isabel
PY  - 2025
UR  - https://uvadoc.uva.es/handle/10324/81675
AB  - Background/Objectives: Genetic variants, such as the µ-opioid receptor 1 (OPRM1) rs1799971 and the catechol-O-methyltransferase (COMT) rs4680, have been considered among the potential causes in the development of some chronic pain conditions. In this...
LA  - spa
PB  - MDPI
KW  - genetic variants
KW  - fibromyalgia
KW  - COMT
KW  - OPRM1
KW  - fatigue
KW  - severity symptoms
KW  - borg scale
KW  - chronic pain
KW  - gender
TI  - Association of Genetic Variants, Such as the μ-Opioid Receptor 1 (OPRM1) rs1799971 and Catechol-O-Methyltransferase (COMT) rs4680, with Phenotypic Expression of Fibromyalgia
DO  - 10.3390/biomedicines13051183
ER  -