Tripolszki, K., Török, D., Goudenège, D., Farkas, K., Sulák, A., Török, N., . . . Széll, M. (2017). High‐throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis. Brain Behav.
Chicago Style citaatTripolszki, Kornélia, et al. "High‐throughput Sequencing Revealed a Novel SETX Mutation in a Hungarian Patient With Amyotrophic Lateral Sclerosis." Brain Behav 2017.
MLA citatieTripolszki, Kornélia, et al. "High‐throughput Sequencing Revealed a Novel SETX Mutation in a Hungarian Patient With Amyotrophic Lateral Sclerosis." Brain Behav 2017.
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