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6. 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. Bouhouche A; Benomar A; Bouslam N; Chkili T; Yahyaoui M J Med Genet; 2006 May; 43(5):441-3. PubMed ID: 16399879 [TBL] [Abstract][Full Text] [Related]
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