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Clinical and Experimental Nephrology|January 27, 2018
Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseasesChina Nagano, Kandai Nozu, Naoya Morisada, et al.
Journal of the American Society of Nephrology : JASN|July 1, 2018
Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport SyndromeTomoko Horinouchi, Kandai Nozu, Tomohiko Yamamura, et al.
Nature Communications|June 4, 2020
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi, et al.
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