De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability.

MLA

Grozeva, Detelina, et al. “De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability.” American Journal of Human Genetics, vol. 94, no. 4, Apr. 2014, pp. 618–24. EBSCOhost, https://doi.org/10.1016/j.ajhg.2014.03.006.

APA

Grozeva, D., Carss, K., Spasic-Boskovic, O., Parker, M., Archer, H., Firth, H., Park, S.-M., Canham, N., Holder, S., Wilson, M., Hackett, A., Field, M., Floyd, J. B., Hurles, M., & Raymond, F. ?Luc. (2014). De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability. American Journal of Human Genetics, 94(4), 618–624. https://doi.org/10.1016/j.ajhg.2014.03.006

Chicago

Grozeva, Detelina, Keren Carss, Olivera Spasic-Boskovic, Michael?J. Parker, Hayley Archer, Helen?V. Firth, Soo-Mi Park, et al. 2014. “De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability.” American Journal of Human Genetics 94 (4): 618–24. doi:10.1016/j.ajhg.2014.03.006.