Kudryashova, E., Struyk, A., Mokhonova, E., Cannon, S. C., & Spencer, M. J. (2011). 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. Oxford University Press.

Kudryashova, Elena, Arie Struyk, Ekaterina Mokhonova, Stephen C. Cannon, ja Melissa J. Spencer. 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. Oxford University Press, 2011.

Kudryashova, Elena, 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. Oxford University Press, 2011.