Individual USH2 proteins make distinct contributions to the ankle link complex during development of the mouse cochlear stereociliary bundle

Usher syndrome (USH) is the leading cause of inherited deaf-blindness, with type 2 (USH2) being the most common clinical form. Studies suggest that proteins encoded by USH2 causative genes assemble into the ankle link complex (ALC) at the hair cell stereociliary bundle; however, little is known abou...

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Bibliographic Details
Published in:Hum Mol Genet
Main Authors: Zou, Junhuang, Mathur, Pranav D., Zheng, Tihua, Wang, Yong, Almishaal, Ali, Park, Albert H., Yang, Jun
Format: Artigo
Language:Inglês
Published: Oxford University Press 2015
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4654051/
https://ncbi.nlm.nih.gov/pubmed/26401052
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv398
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