Article info
PDFElectronic letters
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract
- Correspondence to: Professor A T Moore Institute of Ophthalmology, University College London, 11–43 Bath Street, London, EC1V 9EL, UK; tony.moore{at}ucl.ac.uk
Citation
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract
Publication history
- Accepted June 28, 2005
- Revised June 27, 2005
- First published January 5, 2006.
Online issue publication
April 27, 2016
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Copyright 2006 Journal of Medical Genetics