Recent research identifies gene variants linked to pediatric-onset erythromelalgia, enhancing understanding of this rare condition. The study employs Mendelian and rare-variant association analyses to uncover genetic factors contributing to the disease.
gene variants associated with pediatric onset erythromelalgia mendelian and rare variant association analyses
Original title: “Gene variants associated with pediatric-onset erythromelalgia: Mendelian and rare-variant association analyses.”