• ANO3 (Anoctamin) mutation or DYT24• Spinocerebellar ataxia type-12, type 40• Klinefelter syndrome• Fragile-X tremor ataxia syndrome• Hereditary chin tremor• Charcot-Marie-Tooth disease• Leigh's disease• Mitochondrial polymerase gamma mutation. Here, ANO3 is linked to spinocerebellar ataxia type 12.