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The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins
The hereditary hearing-vision loss disease, Usher syndrome I (USH1), is caused by defects in several proteins that can interact with each other in vitro. Defects in USH1 proteins are thought to be responsible for the developmental and functional impairments of sensory cells in the retina and inner e...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2840103/ https://ncbi.nlm.nih.gov/pubmed/20142502 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0911385107 |
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