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

28 Scopus citations

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Biochemistry, Genetics and Molecular Biology