Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion-Reference-Cited by-同舟云学术

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

Published:2013-11 Issue: Volume:116 Page:371-385
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Kumari Sindhu S.,Gandhi Jason,Mustehsan Mohammed H.,Eren Semih,Varadaraj Kulandaiappan

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference85 articles.

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