Fig. 5: Schematic representation of MFN2 with its most common mutations linked to CMTA2 | Cell Death & Disease

Fig. 5: Schematic representation of MFN2 with its most common mutations linked to CMTA2

From: Mitofusin 2: from functions to disease

Fig. 5

The scheme represents MFN2 protein and depicts amino acid mutations associated to CMT2A. The color refers to the domain affected: red, GTPase domain; blue, HR1/2; green, TM domains; black, linker regions. In bold, the more frequent mutations involving the arginine (R) in position 94

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