Cite
HARVARD Citation
Zhang, N. et al. (2018). Identification of two novel compound heterozygous mutations of ADGRV1 in a Chinese family with Usher syndrome type IIC. Ophthalmic genetics. pp. 517-521. [Online].
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Zhang, N. et al. (2018). Identification of two novel compound heterozygous mutations of ADGRV1 in a Chinese family with Usher syndrome type IIC. Ophthalmic genetics. pp. 517-521. [Online].