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TOPOLOGY OF TRANSMEMBRANE CHANNEL-LIKE GENE 1 PROTEIN (TMC1)
Mutations of transmembrane channel-like gene 1 (TMC1) cause hearing loss in humans and mice. TMC1 is the founding member of a family of genes encoding proteins of unknown function that are predicted to contain multiple transmembrane domains. The goal of our study was to define the topology of mouse...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2010
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3005947/ https://ncbi.nlm.nih.gov/pubmed/20672865 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/bi1004377 |
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