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The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions
Usher syndrome type 1 (USH1) patients suffer from sensorineuronal deafness, vestibular dysfunction, and visual impairment. Several genetic loci have been linked to USH1, and four of the relevant genes have been identified. They encode the unconventional myosin VIIa, the PDZ-domain protein harmonin,...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
2002
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC137525/ https://ncbi.nlm.nih.gov/pubmed/12407180 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.232579599 |
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