Figure 2From: Fabry disease: Identification of 50 novel α-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutationsThe structure of the human α-Gal A monomer based on its X-ray crystal structure. The N- and C-termini are labelled and the active site indicated by a star. The locations of the mutations are shown.Back to article page