Mutations in the PLA2G6 gene (Entrez GeneID:8398) have been identified in autosomal recessive neurodegenerative diseases classified as infantile neuroaxonal dystrophy (INAD), neurodegeneration with brain iron accumulation (NBIA), and dystonia-parkinsonism [1]–[3]. The gene discussed is PLA2G6; the disease is neurodegeneration with brain iron accumulation.