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. (Q36930047)
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scientific article published on 06 January 2006
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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. |
scientific article published on 06 January 2006 |
Statements
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 (English)
Benomar A
Bouslam N
Chkili T
6 January 2006
1 reference
1 reference