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

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Bibliographic Details
Title: Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion.
Authors: Kumari SS; Department of Physiology and Biophysics, Stony Brook University, Stony Brook, NY 11794-8661, USA., Gandhi J, Mustehsan MH, Eren S, Varadaraj K
Source: Experimental eye research [Exp Eye Res] 2013 Nov; Vol. 116, pp. 371-85. Date of Electronic Publication: 2013 Oct 09.
Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Academic Press Country of Publication: England NLM ID: 0370707 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-0007 (Electronic) Linking ISSN: 00144835 NLM ISO Abbreviation: Exp Eye Res Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1096-0007
DOI:10.1016/j.exer.2013.09.019