Functional characterization of a human aquaporin 0 mutation that leads to a congenital dominant lens cataract
Author:
Publisher
Elsevier BV
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference107 articles.
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2. Aquaporin water channels – from atomic structure to clinical medicine;Agre;J. Physiol.,2002
3. Lens structure in MIP-deficient mice;Al-Ghoul;Anat. Rec. A Discov. Mol. Cell Evol. Biol.,2003
4. Water permeability of C-terminally truncated aquaporin 0 (AQP0 1–243) observed in the aging human lens;Ball;Invest. Ophthalmol. Vis. Sci.,2003
5. Lens organelle degradation;Bassnett;Exp. Eye Res.,2002
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