Veeramah, K. R., Johnstone, L., Karafet, T. M., Wolf, D., Sprissler, R., Salogiannis, J., . . . Hammer, M. F. (2013). Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.
Styl cytowania ChicagoVeeramah, Krishna R., et al. Exome Sequencing Reveals New Causal Mutations in Children With Epileptic Encephalopathies. 2013.
Styl cytowania MLAVeeramah, Krishna R., et al. Exome Sequencing Reveals New Causal Mutations in Children With Epileptic Encephalopathies. 2013.
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