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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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Bibliografiske detaljer
Main Authors: Khan, Sehrish Haider, Javed, Muhammad Rizwan, Qasim, Muhammad, Shahzadi, Samar, Jalil, Asma, Rehman, Shahid ur
Format: Artigo
Sprog:Inglês
Udgivet: Biomedical Informatics 2014
Fag:
Online adgang: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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