APA (7th ed.) Citation

LC, N., Y, M., E, M., D, H., K, B., & B, H. (2012). The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein. Human molecular genetics, 21(18), 4038. https://doi.org/10.1093/hmg/dds228

Chicago Style (17th ed.) Citation

LC, Neumann, Markaki Y, Mladenov E, Hoffmann D, Buiting K, and Horsthemke B. "The Imprinted NPAP1/C15orf2 Gene in the Prader-Willi Syndrome Region Encodes a Nuclear Pore Complex Associated Protein." Human Molecular Genetics 21, no. 18 (2012): 4038. https://doi.org/10.1093/hmg/dds228.

MLA (9th ed.) Citation

LC, Neumann, et al. "The Imprinted NPAP1/C15orf2 Gene in the Prader-Willi Syndrome Region Encodes a Nuclear Pore Complex Associated Protein." Human Molecular Genetics, vol. 21, no. 18, 2012, p. 4038, https://doi.org/10.1093/hmg/dds228.