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ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants.
Kloth, K. and Lozic, B. and Tagoe, J. and Hoffer, M.J.V. and Van der Ven, A. and Thiele, H. and Altmüller, J. and Kubisch, C. and Au, P.Y.B. and Denecke, J. and Bijlsma, E.K. and Lessel, D.
Neurogenetics 22 (4): 263-269. October 2021

Genotypic association of exonic LGI4 polymorphisms and childhood absence epilepsy.
Gu, W. and Sander, T. and Becker, T. and Steinlein, O.K.
Neurogenetics 5 (1): 41-44. February 2004

The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.
Wittekindt, O. and Jauch, A. and Burgert, E. and Schaerer, L. and Holtgreve-Grez, H. and Yvert, G. and Imbert, G. and Zimmer, J. and Hoehe, M.R. and Macher, J.P. and Chiaroni, P. and van Calker, D. and Crocq, M.A. and Morris-Rosendahl, D.J.
Neurogenetics 1 (4): 259-265. August 1998