GLA and Fabry disease: These phenotypes, commonly designated by some authors as “cardiac variants” of FD, have been described in association to the GLA mutations p.F113L [4,5,146], p.N215S [147,148,149,150], IVS4+919G>A [151], p.A20P [152], p.I91T [146], p.N139S [153], p.I232T [154], p.I239M [155], p.Q279E [156,157], p.M296I [152,158], p.M296V [159], p.R301Q [156,157,160], and p.G328R [161].