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Abrogation of HMX1 Function Causes Rare Oculoauricular Syndrome Associated With Congenital Cataract, Anterior Segment Dysgenesis, and Retinal Dystrophy
Gillespie, R. L., Urquhart, J., Lovell, S. C., Biswas, S., Parry, N. R. A., Schorderet, D. F., Lloyd, I. C., Clayton-Smith, J., Black, G. C.Volume:
56
Language:
english
Journal:
Investigative Ophthalmology & Visual Science
DOI:
10.1167/iovs.14-15861
Date:
February, 2015
File:
PDF, 1016 KB
english, 2015