Donkervoort, S., Dastgir, J., Hu, Y., Zein, W., Marks, H., Blackstone, C., & Bönnemann, C. G. (2013). Phenotypic variability of a likely FA2H founder mutation in a family with complicated hereditary spastic paraplegia. Clin Genet.
Citação norma ChicagoDonkervoort, Sandra, Jahannaz Dastgir, Ying Hu, Wadih Zein, Harold Marks, Craig Blackstone, and Carsten G. Bönnemann. "Phenotypic Variability of a Likely FA2H Founder Mutation in a Family With Complicated Hereditary Spastic Paraplegia." Clin Genet 2013.
MLA citiranjeDonkervoort, Sandra, et al. "Phenotypic Variability of a Likely FA2H Founder Mutation in a Family With Complicated Hereditary Spastic Paraplegia." Clin Genet 2013.
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