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USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23
Usher syndrome (USH) is a hereditary disorder associated with sensorineural hearing impairment, progressive loss of vision attributable to retinitis pigmentosa and variable vestibular function. Three clinical types have been described with type I (USH1) being the most severe. To date six USH1 loci h...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2673543/ https://ncbi.nlm.nih.gov/pubmed/18505454 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2008.01038.x |
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