Cite
APA Citation
Wormser, O., Gradstein, L., Kadar, E., Yogev, Y., Perez, Y., Mashkit, E., Elbedour, K., Drabkin, M., Markus, B., Kadir, R., Halperin, D., Khalaila, S., Levy, J., Lifshitz, T., Manor, E., & Birk, O. S. (2018). combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe. American journal of medical genetics, 176(12), 2695–2703. http://access.bl.uk/ark:/81055/vdc_100076766164.0x000021