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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...
Gorde:
| Egile Nagusiak: | , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Biomedical Informatics
2014
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| Gaiak: | |
| Sarrera elektronikoa: | 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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