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The unconventional myosin-VIIa associates with lysosomes
Mutations in the myosin-VIIa (MYO7a) gene cause human Usher disease, characterized by hearing impairment and progressive retinal degeneration. In the retina, myosin-VIIa is highly expressed in the retinal pigment epithelium, where it plays a role in the positioning of melanosomes and other digestion...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2005
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1201382/ https://ncbi.nlm.nih.gov/pubmed/16001398 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cm.20080 |
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