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. Author manuscript; available in PMC: 2022 Mar 1.
Published in final edited form as: Trends Cell Biol. 2020 Dec 1;31(3):197–210. doi: 10.1016/j.tcb.2020.11.003

Figure 2: FKRP mutations associated with dystroglycanopathies.

Figure 2:

Linear representation of fukutin related protein (FKRP) protein and different unique pathological amino acid variants associated with misssense or framseshift mutations as described in the Leiden database. FKRP-related limb-girdle muscular dystrophy (LGMDR9) only in blue, FKRP-related congenital muscular dystrophy (MDC1C) in orange, Walker-Warburg Syndrome (WWS)/muscle eye brain disease (MEB) in yellow. Green shows mutations associated with LGMDR9 and MDC1C, purple mutations associated with MDC1C and WWS/MEB and the red residues are associated with LGMDR9, MDC1C and WWS/MEB.