1. Van Bogaert, Patrick. . KCTD7-related progressive myoclonus epilepsy. In Epileptic disorders : international epilepsy journal with videotape, 18, 115-119. doi:. https://pubmed.ncbi.nlm.nih.gov/27629772/
2. Alevy, Jonathan, Burger, Courtney A, Albrecht, Nicholas E, Jiang, Danye, Samuel, Melanie A. 2019. Progressive myoclonic epilepsy-associated gene Kctd7 regulates retinal neurovascular patterning and function. In Neurochemistry international, 129, 104486. doi:10.1016/j.neuint.2019.104486. https://pubmed.ncbi.nlm.nih.gov/31175897/
3. Wang, Yalan, Cao, Xiaotong, Liu, Pei, Wang, Chenji, Wang, Hongyan. 2022. KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses. In Science advances, 8, eabm5578. doi:10.1126/sciadv.abm5578. https://pubmed.ncbi.nlm.nih.gov/35921411/
4. Chia, Ruth, Ray, Anindita, Shah, Zalak, Houlden, Henry, Scholz, Sonja W. 2024. Genome sequence analyses identify novel risk loci for multiple system atrophy. In Neuron, 112, 2142-2156.e5. doi:10.1016/j.neuron.2024.04.002. https://pubmed.ncbi.nlm.nih.gov/38701790/
5. Teng, Xinchen, Aouacheria, Abdel, Lionnard, Loïc, Kamiya, Atsushi, Hardwick, J Marie. . KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders. In CNS neuroscience & therapeutics, 25, 887-902. doi:10.1111/cns.13156. https://pubmed.ncbi.nlm.nih.gov/31197948/
6. Liang, Justine H, Alevy, Jonathan, Akhanov, Viktor, Noebels, Jeffrey L, Samuel, Melanie A. 2022. Kctd7 deficiency induces myoclonic seizures associated with Purkinje cell death and microvascular defects. In Disease models & mechanisms, 15, . doi:10.1242/dmm.049642. https://pubmed.ncbi.nlm.nih.gov/35972048/
智鼠故事 
