Elena. Kudryashova, et.al., The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype., Human molecular genetics, 2011, 20
Elena. Kudryashova, et.al., The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype., Human molecular genetics, 2011, 20