Churchill, J. D., Bowne, S. J., Sullivan, L. S., Lewis, R. A., Wheaton, D. K., Birch, D. G., . . . Daiger, S. P. (2013). Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa. The Association for Research in Vision and Ophthalmology.

Churchill, Jennifer D., Sara J. Bowne, Lori S. Sullivan, Richard Alan Lewis, Dianna K. Wheaton, David G. Birch, Kari E. Branham, John R. Heckenlively, and Stephen P. Daiger. Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5% of Families With a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa. The Association for Research in Vision and Ophthalmology, 2013.

Churchill, Jennifer D., et al. Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5% of Families With a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa. The Association for Research in Vision and Ophthalmology, 2013.