Exome Sequencing Identifies a Founder Frameshift Mutation in an Alternative Exon of USH1C as the Cause of Autosomal Recessive Retinitis Pigmentosa with Late-Onset Hearing Loss

Samer Khateb, Lina Zelinger, Tamar Ben-Yosef, Saul Merin, Ornit Crystal-Shalit, Menachem Gross, Eyal Banin*, Dror Sharon

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

27 Scopus citations

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Biochemistry, Genetics and Molecular Biology

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