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121 Jiang et al 122 have identified the GSTM3 variant in the people of Taiwan region, China as a novel genetic modifier in Brugada syndrome, a condition associated with an increased risk of sudden cardiac death

doi: 10.1007/s592-001-8076-6

Statistics and reproducibility In our study, we utilized R version 4.2.1 and conducted data analysis in the RStudio integrated development environment (version 2022.12.0-353)

Nevertheless, a European guideline recommends that eGFR should be monitored in at least 3-month intervals in children with CKD started on rhGH treatment, and that treatment should be discontinued in patients presenting with an unexplained decline in eGFR [154]