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Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma

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Description scientific article
Author/s

author: Ian M. Carr  Adam K Rudkin  James A Poulter  Kathryn P. Burdon  Chris F. Inglehearn  Narcis Fernandez-Fuentes  Carmel Toomes  Jamie E Craig  Clare Victoria Logan  David Parry  Eamonn Sheridan 

Publication date September 1, 2011
Language English
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