Badv, R. S., Shariatmadari, F., Bayat, S., Memarian, S., Esteghamat Hanzae, S., & Yousefimanesh, H. (2024). A case of a 6-year-old girl with a rare compound heterozygous mutation of KCTD7 presenting with progressive myoclonic epilepsy. Egyptian Journal of Medical Human Genetics, 25(1), 1-4. https://doi.org/10.1186/s43042-024-00603-5

Badv, Reza Shervin, Fakhreddin Shariatmadari, Shiva Bayat, Sara Memarian, Samaneh Esteghamat Hanzae, and Hossein Yousefimanesh. "A Case of a 6-year-old Girl with a Rare Compound Heterozygous Mutation of KCTD7 Presenting with Progressive Myoclonic Epilepsy." Egyptian Journal of Medical Human Genetics 25, no. 1 (2024): 1-4. https://doi.org/10.1186/s43042-024-00603-5.

Badv, Reza Shervin, et al. "A Case of a 6-year-old Girl with a Rare Compound Heterozygous Mutation of KCTD7 Presenting with Progressive Myoclonic Epilepsy." Egyptian Journal of Medical Human Genetics, vol. 25, no. 1, 2024, pp. 1-4, https://doi.org/10.1186/s43042-024-00603-5.