APA (7th ed.) Citation

Dohrn, M. F., Kotzaeridou, U., & Korenke, C. (2017). Frequent genes in rare diseases: Panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies. Journal of neurochemistry, 143(5), . https://doi.org/10.1111/jnc.14217

Chicago Style (17th ed.) Citation

Dohrn, Maike F., Urania Kotzaeridou, and Christoph Korenke. "Frequent Genes in Rare Diseases: Panel-based Next Generation Sequencing to Disclose Causal Mutations in Hereditary Neuropathies." Journal of Neurochemistry 143, no. 5 (2017). https://doi.org/10.1111/jnc.14217.

MLA (9th ed.) Citation

Dohrn, Maike F., et al. "Frequent Genes in Rare Diseases: Panel-based Next Generation Sequencing to Disclose Causal Mutations in Hereditary Neuropathies." Journal of Neurochemistry, vol. 143, no. 5, 2017, https://doi.org/10.1111/jnc.14217.