Fig. 3From: Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disordersPOMT1 mutations detected in patients of this study. Mutations can be located in the cytoplasma, in transmembranous domains, or in the endoplasmatic reticulum (ER). MIR: motif in overlapping homologous superfamilies (IPR016093)Back to article page