Teng X, et al. (2019) KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders. CNS Neurosci Ther 25(7):887-902 PMID:31197948
Metz KA, et al. (2018) KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect. Ann Neurol 84(5):766-780 PMID:30295347