Work Cited

Bui, D. (n.d.). The Genetic Cure. Retrieved March 28, 2017, from http://gencure46.wixsite.com/genetic-revolution/issues-and-impacts-cni3

Cepko, C. L. (2012). Emerging gene therapies for retinal degenerations. The Journal Of Neuroscience, 32(19), 6415-6420. doi:10.1523/JNEUROSCI.0295-12.2012

Color Blindness [Color spectrum ]. (2009, September 26). Retrieved April 20, 2017, from https://commons.wikimedia.org/wiki/File:Color_blindness.png

Color Blindness Tests. (n.d.). Retrieved February 28, 2017

Eight Ishihara charts for testing colour blindness, Europe Wellcome L0059163 [Ishihara test]. (2016, March 21). Retrieved April 20, 2017, from https://commons.wikimedia.org/wiki/File:Eight_Ishihara_charts_for_testing_colour_blindness,_Europe_Wellcome_L0059163.jpg

GeneCard. (n.d.). [Variations in CNGA3]. Retrieved May 1, 2017, from http://www.genecards.org/cgi-bin/carddisp.pl?gene=CNGA3&keywords=CNGA3

Gene Therapy Marches Toward CURES for Inherited Blindness. (2011). Research at Penn, 98-9.

GNAT2 G protein subunit alpha transducin 2 [Homo sapiens (human)] - Gene - NCBI. (2017, February 20). Retrieved March 02, 2017.

Graetzer, H. P. (2017). Color blindness. Magill’S Medical Guide (Online Edition).

Hauswirth, W. W. (2014, June). TOXNET. Retrieved May 01, 2017, from https://toxnet.nlm.nih.gov/cgi-bin/sis/search2/f?.%2Ftemp%2F~KLc5Te%3A1

Katagiri, Satoshi, et al. "Congenital Achromatopsia And Macular Atrophy Caused By A Novel Recessive PDE6C Mutation (P.E591K)." Ophthalmic Genetics 36.2 (2015): 137-144. Academic Search Complete. Web. 9 Feb. 2017.

Kohl, S., & Hamel, C. P. (2011). Clinical utility gene card for: achromatopsia. European Journal Of Human Genetics: EJHG, 19(6), doi:10.1038/ejhg.2010.231

Mallen, P. (n.d.). AAV Retinal Targeting Following Subretinal Injection [Digital image]. Retrieved May 1, 2017, from http://www.vdb-lab.org/about/

Mancuso, K., Hauswirth, W. W., Qiuhong, L., Connor, T. B., Kuchenbecker, J. A., Mauck, M. C., & ... Neitz, M. (2009). Gene therapy for red–green colour blindness in adult primates. Nature, 461(7265), 784-787. doi:10.1038/nature08401

Mandal, M. D. (2014, January 14). Gene Therapy Issues. Retrieved March 28, 2017, from http://www.news-medical.net/health/Gene-Therapy-Issues.aspx

Nathans, J., Piantanida, T. P., & Eddy, R. L. (1986). Molecular genetics of inherited variation in human color vision. Science, 232203-210.

Ouechtati, F., Merdassi, A., Bouyacoub, Y., Largueche, L., Derouiche, K., Ouragini, H., & ... El Matri, L. (n.d). Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene. Journal Of Human Genetics, 56(1), 22-28.

Schon, C., Biel, M., & Michalakis, S. (2013, March 28). Gene replacement therapy for retinal CNG channelopathies. Molecular Genetics And Genomics, 288(10), 459-467.

Schon, C., Biel, M., & Michalakis, S. (2013, March 28). Gene Therapy CNGA3 [Confocal Retinal Images]. Retrieved April 24, 2017. DOI 10.1007/s00438-013-0766-4

Schon, C., Biel, M., & Michalakis, S. (2013, March 28). Gene Therapy CNGB1 [Confocal Retinal Images]. Retrieved April 24, 2017. DOI 10.1007/s00438-013-0766-4

The Impacts and Issues. (n.d.). Retrieved March 28, 2017, from http://gene-therapy.yolasite.com/concerns-and-controversy.php





Introduction
Materials and Methods
Broader Impacts
Results
Discussion