Cite
Abnormal neurodevelopment outcome in case of neonatal hyperekplexia secondary to missense mutation in GLRB gene.
MLA
Gupta, Naveen Parkash, et al. “Abnormal Neurodevelopment Outcome in Case of Neonatal Hyperekplexia Secondary to Missense Mutation in GLRB Gene.” BMJ Case Reports, vol. 13, no. 12, Dec. 2020. EBSCOhost, https://doi.org/10.1136/bcr-2020-236152.
APA
Gupta, N. P., Verma, V., Chopra, S., & Choudhury, V. (2020). Abnormal neurodevelopment outcome in case of neonatal hyperekplexia secondary to missense mutation in GLRB gene. BMJ Case Reports, 13(12). https://doi.org/10.1136/bcr-2020-236152
Chicago
Gupta, Naveen Parkash, Vinita Verma, Saurabh Chopra, and Vivek Choudhury. 2020. “Abnormal Neurodevelopment Outcome in Case of Neonatal Hyperekplexia Secondary to Missense Mutation in GLRB Gene.” BMJ Case Reports 13 (12). doi:10.1136/bcr-2020-236152.