A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis

Overview of attention for article published in Japanese Journal of Ophthalmology, August 2014

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A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis. https://t.co/CW6SUOXFLX

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