Cite
HARVARD Citation
Cheng, J. et al. (2019). A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree. Journal of cellular and molecular medicine. 23 (5), pp. 3776-3780. [Online].
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Cheng, J. et al. (2019). A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree. Journal of cellular and molecular medicine. 23 (5), pp. 3776-3780. [Online].