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Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion

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第一作者： Kumari,S.S.

作者： Kumari,S.S. ^[1] ; Gandhi,J. ; Mustehsan,M.H. ; Eren,S. ; Varadaraj,K.

作者单位： Department of Physiology and Biophysics, Stony Brook University, Stony Brook, NY 11794-8661, United ^[1]

关键词 AQP0 Cell-to-cell adhesion Congenital cataract Connexin 50 Trafficking Water channel Water permeability

发布时间 2014-03-06

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Experimental Eye Research

2013年116卷

371-385页

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2013年116卷

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Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion

Experimental Eye Research

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Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion

Experimental Eye Research

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Experimental Eye Research

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