APA (7th ed.) Citation

Scholz, C., Golas, M. M., Weber, R. G., Hartmann, C., Lehmann, U., Sahm, F., . . . Hofmann, W. (2018). Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia-oculomotor apraxia 4 and pilocytic astrocytoma. Clinical genetics, 94(1), . https://doi.org/10.1111/cge.13216

Chicago Style (17th ed.) Citation

Scholz, Christian, et al. "Rare Compound Heterozygous Variants in PNKP Identified by Whole Exome Sequencing in a German Patient with Ataxia-oculomotor Apraxia 4 and Pilocytic Astrocytoma." Clinical Genetics 94, no. 1 (2018). https://doi.org/10.1111/cge.13216.

MLA (9th ed.) Citation

Scholz, Christian, et al. "Rare Compound Heterozygous Variants in PNKP Identified by Whole Exome Sequencing in a German Patient with Ataxia-oculomotor Apraxia 4 and Pilocytic Astrocytoma." Clinical Genetics, vol. 94, no. 1, 2018, https://doi.org/10.1111/cge.13216.