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Domain analyses of Usher syndrome causing Clarin-1 and GPR98 protein models
Usher syndrome is an autosomal recessive disorder that causes hearing loss, Retinitis Pigmentosa (RP) and vestibular dysfunction. It is clinically and genetically heterogeneous disorder which is clinically divided into three types i.e. type I, type II and type III. To date, there are about twelve lo...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Biomedical Informatics
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4166767/ https://ncbi.nlm.nih.gov/pubmed/25258483 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6026/97320630010491 |
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