APA (7th ed.) Citation

NJ, L., LE, F., DA, S., MT, R., SE, C., VK, M., . . . DR, T. (2019). A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein-truncating variant. Human mutation, 40(7), 893. https://doi.org/10.1002/humu.23753

Chicago Style (17th ed.) Citation

NJ, Lake, et al. "A Patient with Homozygous Nonsense Variants in Two Leigh Syndrome Disease Genes: Distinguishing a Dual Diagnosis from a Hypomorphic Protein-truncating Variant." Human Mutation 40, no. 7 (2019): 893. https://doi.org/10.1002/humu.23753.

MLA (9th ed.) Citation

NJ, Lake, et al. "A Patient with Homozygous Nonsense Variants in Two Leigh Syndrome Disease Genes: Distinguishing a Dual Diagnosis from a Hypomorphic Protein-truncating Variant." Human Mutation, vol. 40, no. 7, 2019, p. 893, https://doi.org/10.1002/humu.23753.