Cite
MLA Citation
Ohad Wormser et al.. “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, vol. 176, no. 12, 2018, pp. 2695–2703. http://access.bl.uk/ark:/81055/vdc_100076766164.0x000021