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Mutations in HspB1 and hereditary neuropathies
Charcot-Marie-Tooth (CMT) disease is major hereditary neuropathy. CMT has been linked to mutations in a range of proteins, including the small heat shock protein HspB1. Here we review the properties of several HspB1 mutants associated with CMT. In vitro, mutations in the N-terminal domain lead to a...
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| Publicado no: | Cell Stress Chaperones |
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| Principais autores: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Netherlands
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7332652/ https://ncbi.nlm.nih.gov/pubmed/32301006 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12192-020-01099-9 |
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