Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.

MLA

Padhi, Evin M., et al. “Coding and Noncoding Variants in EBF3 Are Involved in HADDS and Simplex Autism.” Human Genomics, vol. 15, no. 1, July 2021, p. 44. EBSCOhost, https://doi.org/10.1186/s40246-021-00342-3.

APA

Padhi, E. M., Hayeck, T. J., Cheng, Z., Chatterjee, S., Mannion, B. J., Byrska-Bishop, M., Willems, M., Pinson, L., Redon, S., Benech, C., Uguen, K., Audebert-Bellanger, S., Le Marechal, C., Férec, C., Efthymiou, S., Rahman, F., Maqbool, S., Maroofian, R., Houlden, H., … Turner, T. N. (2021). Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. Human Genomics, 15(1), 44. https://doi.org/10.1186/s40246-021-00342-3

Chicago

Padhi, Evin M, Tristan J Hayeck, Zhang Cheng, Sumantra Chatterjee, Brandon J Mannion, Marta Byrska-Bishop, Marjolaine Willems, et al. 2021. “Coding and Noncoding Variants in EBF3 Are Involved in HADDS and Simplex Autism.” Human Genomics 15 (1): 44. doi:10.1186/s40246-021-00342-3.