Tripolszki Kornélia, Török Dóra, Goudenège David, Farkas Katalin, Sulák Adrienn, Török Nóra, . . . Széll Márta. (2017). High- throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis.
Chicago Style (17th ed.) CitationTripolszki Kornélia, et al. High- Throughput Sequencing Revealed a Novel SETX Mutation in a Hungarian Patient with Amyotrophic Lateral Sclerosis. Wiley, 2017.
MLA idézésTripolszki Kornélia, et al. High- Throughput Sequencing Revealed a Novel SETX Mutation in a Hungarian Patient with Amyotrophic Lateral Sclerosis. 2017.
Figyelem: ezek az hivatkozások nem 100%-ban pontosak..