APA (7th ed.) Citation

Helbig, K. L., Hedrich, U. B., Shinde, D. N., Krey, I., Teichmann, A., Hentschel, J., . . . Lehesjoki, A. (2016). A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. Annals of Neurology, 80(4), n/a. https://doi.org/10.1002/ana.24762

Chicago Style (17th ed.) Citation

Helbig, Katherine L., et al. "A Recurrent Mutation in KCNA2 as a Novel Cause of Hereditary Spastic Paraplegia and Ataxia." Annals of Neurology 80, no. 4 (2016): n/a. https://doi.org/10.1002/ana.24762.

MLA (9th ed.) Citation

Helbig, Katherine L., et al. "A Recurrent Mutation in KCNA2 as a Novel Cause of Hereditary Spastic Paraplegia and Ataxia." Annals of Neurology, vol. 80, no. 4, 2016, p. n/a, https://doi.org/10.1002/ana.24762.