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The many different cellular functions of MYO7A in the retina
Mutations in MYO7A cause Usher syndrome type 1B, a disorder involving profound congenital deafness and progressive blindness. In the retina, most of MYO7A is localized in the apical region of the RPE (retinal pigmented epithelial) cells, and a small amount is associated with the ciliary and pericili...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3703834/ https://ncbi.nlm.nih.gov/pubmed/21936790 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST0391207 |
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