. . . . . "CCT5" . . . . "Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia." . . . . "2018-04-05T10:17:11.353+02:00"^^ . . . . . .