1. Aslan-Kara, Kezban, Dündar-Yenilmez, Ebru, Ateş, Elçin, Bozdemir, Hacer, Tuli, Abdullah. 2023. EFHC1 gene mutation profile of Turkish JME patients and its association with disease risk. In Seizure, 114, 79-83. doi:10.1016/j.seizure.2023.12.002. https://pubmed.ncbi.nlm.nih.gov/38088014/
2. Conte, Fábio F, Ribeiro, Patrícia A O, Marchesini, Rafael B, Bittencourt, Jackson C, Lopes-Cendes, Iscia. 2009. Expression profile and distribution of Efhc1 gene transcript during rodent brain development. In Journal of molecular neuroscience : MN, 39, 69-77. doi:10.1007/s12031-009-9179-6. https://pubmed.ncbi.nlm.nih.gov/19191033/
3. Thounaojam, Romita, Langbang, Leader, Itisham, Kavish, Tripathi, Manjari, Aguan, Kripamoy. 2017. EFHC1 mutation in Indian juvenile myoclonic epilepsy patient. In Epilepsia open, 2, 84-89. doi:10.1002/epi4.12037. https://pubmed.ncbi.nlm.nih.gov/29750216/
4. Raju, Praveen K, Satishchandra, Parthasarathy, Nayak, Sourav, Sinha, Sanjib, Anand, Anuranjan. 2017. Microtubule-associated defects caused by EFHC1 mutations in juvenile myoclonic epilepsy. In Human mutation, 38, 816-826. doi:10.1002/humu.23221. https://pubmed.ncbi.nlm.nih.gov/28370826/
5. Yamakawa, Kazuhiro, Suzuki, Toshimitsu. . Re-evaluation of myoclonin1 immunosignals in neuron, mitotic spindle, and midbody--nonspecific? In Epilepsy & behavior : E&B, 28 Suppl 1, S61-2. doi:10.1016/j.yebeh.2012.06.032. https://pubmed.ncbi.nlm.nih.gov/23756482/
6. Suzuki, Toshimitsu, Inoue, Ikuyo, Yamakawa, Kazuhiro. 2020. Epilepsy protein Efhc1/myoclonin1 is expressed in cells with motile cilia but not in neurons or mitotic apparatuses in brain. In Scientific reports, 10, 22076. doi:10.1038/s41598-020-79202-4. https://pubmed.ncbi.nlm.nih.gov/33328576/