APA (7th ed.) Citation

Kunii, M., Doi, H., Higashiyama, Y., Kugimoto, C., Ueda, N., Hirata, J., . . . Tanaka, F. (2015). A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation. Journal of Human Genetics, 60(4), 187. https://doi.org/10.1038/jhg.2015.7

Chicago Style (17th ed.) Citation

Kunii, Misako, et al. "A Japanese Case of Cerebellar Ataxia, Spastic Paraparesis and Deep Sensory Impairment Associated with a Novel Homozygous TTC19 Mutation." Journal of Human Genetics 60, no. 4 (2015): 187. https://doi.org/10.1038/jhg.2015.7.

MLA (9th ed.) Citation

Kunii, Misako, et al. "A Japanese Case of Cerebellar Ataxia, Spastic Paraparesis and Deep Sensory Impairment Associated with a Novel Homozygous TTC19 Mutation." Journal of Human Genetics, vol. 60, no. 4, 2015, p. 187, https://doi.org/10.1038/jhg.2015.7.