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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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Bibliografische gegevens
Hoofdauteurs: Yan, Jing, Pan, Lifeng, Chen, Xiuye, Wu, Lin, Zhang, Mingjie
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: National Academy of Sciences 2010
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Online toegang: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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