Edwards, R., Murphy, G., Owens, J. W., Erickson, C., Hopkin, R., Shillington, A., & Das, S. P. (2025). Dual Diagnosis of Fragile X Syndrome and DEPDC5‐Related Disorder Emphasizes DEPDC5's Role Beyond Familial Epilepsy: A Case Report and Literature Review. Case Reports in Genetics, 2025, 1. https://doi.org/10.1155/crig/4501466
Chicago Style (17th ed.) CitationEdwards, Rory, Grace Murphy, Joshua W. Owens, Craig Erickson, Robert Hopkin, Amelle Shillington, and Sofia Priyadarsani Das. "Dual Diagnosis of Fragile X Syndrome and DEPDC5‐Related Disorder Emphasizes DEPDC5's Role Beyond Familial Epilepsy: A Case Report and Literature Review." Case Reports in Genetics 2025 (2025): 1. https://doi.org/10.1155/crig/4501466.
MLA (9th ed.) CitationEdwards, Rory, et al. "Dual Diagnosis of Fragile X Syndrome and DEPDC5‐Related Disorder Emphasizes DEPDC5's Role Beyond Familial Epilepsy: A Case Report and Literature Review." Case Reports in Genetics, vol. 2025, 2025, p. 1, https://doi.org/10.1155/crig/4501466.