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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
BACKGROUND: Mutilating sensory neuropathy with spastic paraplegia is a very rare disease with both autosomal dominant and recessive modes of inheritance. We previously mapped the locus of the autosomal recessive form to a 25 cM interval between markers D5S2048 and D5S648 on chromosome 5p. In this ca...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2564519/ https://ncbi.nlm.nih.gov/pubmed/16399879 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.039230 |
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