Cite
HARVARD Citation
Imani, S. et al. (2018). Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing. Journal of cellular and molecular medicine. 22 (3), pp. 1733-1742. [Online].
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Imani, S. et al. (2018). Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing. Journal of cellular and molecular medicine. 22 (3), pp. 1733-1742. [Online].