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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Detalles Bibliográficos
Autores principales: Khan, Sehrish Haider, Javed, Muhammad Rizwan, Qasim, Muhammad, Shahzadi, Samar, Jalil, Asma, Rehman, Shahid ur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2014
Materias:
Hypothesis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166767/
https://www.ncbi.nlm.nih.gov/pubmed/25258483
http://dx.doi.org/10.6026/97320630010491

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166767/
https://www.ncbi.nlm.nih.gov/pubmed/25258483
http://dx.doi.org/10.6026/97320630010491

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