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Characterization of the Drosophila Ortholog of the Human Usher Syndrome Type 1G Protein Sans
BACKGROUND: The Usher syndrome (USH) is the most frequent deaf-blindness hereditary disease in humans. Deafness is attributed to the disorganization of stereocilia in the inner ear. USH1, the most severe subtype, is associated with mutations in genes encoding myosin VIIa, harmonin, cadherin 23, prot...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2009
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2649435/ https://www.ncbi.nlm.nih.gov/pubmed/19270738 http://dx.doi.org/10.1371/journal.pone.0004753 |