Cite
HARVARD Citation
Fu, Q. et al. (2017). CEP78 is mutated in a distinct type of Usher syndrome. Journal of medical genetics. 54 (3), pp. 190-195. [Online].
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Fu, Q. et al. (2017). CEP78 is mutated in a distinct type of Usher syndrome. Journal of medical genetics. 54 (3), pp. 190-195. [Online].