OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium
Vincent, A., Forster, N., Maynes, J. T., Paton, T. A., Billingsley, G., Roslin, N. M., Ali, A., Sutherland, J., Wright, T., Westall, C. A., Paterson, A. D., Marshall, C. R., Heon, E., Boycott, K., FriVolume:
51
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2014-102620
Date:
December, 2014
File:
PDF, 3.38 MB
english, 2014