Of these, ABHD12, VPS11, ATX10, AFG3L2, and ROGDI are all associated with neurological disorders (respectively, PHARC syndrome (53), hypomyelinating leukodystrophy 12 (54), spinocerebellar ataxia type 10 (59) and 28 (56, 60), and Kohlschutter’s syndrome (58)) (supplemental Table S6). The gene discussed is AFG3L2; the disease is spinocerebellar ataxia type 10.