APA (7th ed.) Citation

Latsko, M. S., Koboldt, D. C., Franklin, S. J., Hickey, S. E., Williamson, R. K., Garner, S., . . . Wilson, R. K. (2022). De novo missense variant in GRIA2 in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy. Cold Spring Harbor molecular case studies, 8(4), 1. https://doi.org/10.1101/mcs.a006172

Chicago Style (17th ed.) Citation

Latsko, Maeson S., et al. "De Novo Missense Variant in GRIA2 in a Patient with Global Developmental Delay, Autism Spectrum Disorder, and Epileptic Encephalopathy." Cold Spring Harbor Molecular Case Studies 8, no. 4 (2022): 1. https://doi.org/10.1101/mcs.a006172.

MLA (9th ed.) Citation

Latsko, Maeson S., et al. "De Novo Missense Variant in GRIA2 in a Patient with Global Developmental Delay, Autism Spectrum Disorder, and Epileptic Encephalopathy." Cold Spring Harbor Molecular Case Studies, vol. 8, no. 4, 2022, p. 1, https://doi.org/10.1101/mcs.a006172.