Genetics in Medicine Open (Jan 2023)

P459: Exome sequencing analysis reveals enrichment of variants in known autosomal dominant hearing loss genes in patients with presbycusis

  • Stefan Farrugia,
  • Rory Olson,
  • Eric Klee,
  • Lisa Schimmenti

Journal volume & issue
Vol. 1, no. 1
p. 100506

Abstract

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No abstracts available.