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Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain
Protocadherin 15 (PCDH15) is expressed in hair cells of the inner ear and in photoreceptors of the retina. Mutations in PCDH15 cause Usher Syndrome (deaf-blindness) and recessive deafness. In developing hair cells, PCDH15 localizes to extracellular linkages that connect the stereocilia and kinociliu...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Company of Biologists
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3062428/ https://ncbi.nlm.nih.gov/pubmed/21427143 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.060061 |
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