Rinaldi, C., Schmidt, T., Situ, A. J., Johnson, J. O., Lee, P. R., Chen, K., . . . Fischbeck, K. H. (2015). Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia. JAMA Neurol.
Chicago Style aipamenaRinaldi, Carlo, et al. "Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia." JAMA Neurol 2015.
MLA aipamenaRinaldi, Carlo, et al. "Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia." JAMA Neurol 2015.
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