| 1 | CCT5, ELP1, HSAN1, HSAN2A, HSAN3, HSAN4, HSAN5, NGF, NTRK1, SNSP, SPTLC1, WNK1 |
| Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. | |
| Rotthier A, Baets J, De Vriendt E, Jacobs A, Auer-Grumbach M, Lévy N, Bonello-Palot N, Kilic SS, Weis J, Nascimento A, Swinkels M, Kruyt MC, Jordanova A, De Jonghe P, Timmerman V. | |
| Brain 132(Pt 10):2699-711. Epub 2009 Aug 3.PMID: 19651702 2009 | |
| 2 | CCT5, SNSP |
| 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 43(5):441-3. Epub 2006 Jan 6. 2006 | |