GLA and Fabry disease: Among the cases of FD identified in this study, we found ten previously reported GLA mutations (p.L68F,18 p.R301Q,19 p.Q312R,20 p.R112H,21 p.K391E,22 p.R220P,23 p.D231N,24 p.L415P,25 p.N263S,26 and p.L403S).20 Two other mutations were identified—i.e., p.G85V and the frameshift mutation c.559_560delAT—and both probands were classified as the classic type.