APA (7th ed.) Citation

Evers, C., Kaufmann, L., Seitz, A., Paramasivam, N., Granzow, M., Karch, S., . . . Moog, U. (2016). Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy. American journal of medical genetics, 170(6), . https://doi.org/10.1002/ajmg.a.37632

Chicago Style (17th ed.) Citation

Evers, Christina, et al. "Exome Sequencing Reveals a Novel CWF19L1 Mutation Associated with Intellectual Disability and Cerebellar Atrophy." American Journal of Medical Genetics 170, no. 6 (2016). https://doi.org/10.1002/ajmg.a.37632.

MLA (9th ed.) Citation

Evers, Christina, et al. "Exome Sequencing Reveals a Novel CWF19L1 Mutation Associated with Intellectual Disability and Cerebellar Atrophy." American Journal of Medical Genetics, vol. 170, no. 6, 2016, https://doi.org/10.1002/ajmg.a.37632.