AK, A., SD, S., DT, T., EG, W., RK, O., JC, D., . . . JR, G. (2017). Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. Human genetics, 136(11-12), 1395. https://doi.org/10.1007/s00439-017-1838-z
Chicago Style (17th ed.) CitationAK, Adams, Smith SD, Truong DT, Willcutt EG, Olson RK, DeFries JC, Pennington BF, and Gruen JR. "Enrichment of Putatively Damaging Rare Variants in the DYX2 Locus and the Reading-related Genes CCDC136 and FLNC." Human Genetics 136, no. 11-12 (2017): 1395. https://doi.org/10.1007/s00439-017-1838-z.
MLA (9th ed.) CitationAK, Adams, et al. "Enrichment of Putatively Damaging Rare Variants in the DYX2 Locus and the Reading-related Genes CCDC136 and FLNC." Human Genetics, vol. 136, no. 11-12, 2017, p. 1395, https://doi.org/10.1007/s00439-017-1838-z.