More recently, Dhoke and colleagues [92] documented a universal gene correction approach for fukutin-related protein (FKRP), whose mutations are associated with a broad spectrum of muscular dystrophies, including LGMD type 2I (LGMD2I/R9) and the severe Walker-Warburg syndrome (WWS). Here, FKRP is linked to muscular dystrophy-dystroglycanopathy, type A.