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APA Citation
Zhang, N., Wang, J., Liu, S., Liu, M., & Jiang, F. (2018). identification of two novel compound heterozygous mutations of ADGRV1 in a Chinese family with Usher syndrome type IIC. Ophthalmic genetics, 39, 517–521. http://access.bl.uk/ark:/81055/vdc_100066523668.0x000022