In addition, although TGFBR3 c.568+1G>A would lead to a PTC triggering NMD, the circumstances of death showing possible myocardial infarction in the autopsy and this gene has been associated with Marfan syndrome in a single publication, though there is limited evidence to support this gene disease association [12]. The gene discussed is TGFBR3; the disease is myocardial infarction.