APA (7th ed.) Citation

Srour, M., Hamdan, F. F., Gan‐Or, Z., Labuda, D., Nassif, C., Oskoui, M., . . . Michaud, J. (2015). A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly. Clinical Genetics, 88(1), E1. https://doi.org/10.1111/cge.12605

Chicago Style (17th ed.) Citation

Srour, M., et al. "A Homozygous Mutation in SLC1A4 in Siblings with Severe Intellectual Disability and Microcephaly." Clinical Genetics 88, no. 1 (2015): E1. https://doi.org/10.1111/cge.12605.

MLA (9th ed.) Citation

Srour, M., et al. "A Homozygous Mutation in SLC1A4 in Siblings with Severe Intellectual Disability and Microcephaly." Clinical Genetics, vol. 88, no. 1, 2015, p. E1, https://doi.org/10.1111/cge.12605.