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APA Citation
Gupta, S., Chaurasia, A., Pathak, E., Mishra, R., Chaudhry, V. N., Chaudhry, P., Mukherjee, A., & Mutsuddi, M. (2017). whole exome sequencing unveils a frameshift mutation in CNGB3 for cone dystrophy. Medicine, 96(30), . http://access.bl.uk/ark:/81055/vdc_100048092176.0x00004e