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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
Affiliations
Stefan Farrugia
Mayo Clinic Alix School of Medicine
Rory Olson
Mayo Clinic, Center for Individualized Medicine
Eric Klee
Mayo Clinic, Center for Individualized Medicine
Lisa Schimmenti
Mayo Clinic, Department of Clinical Genomics
Journal volume & issue
Vol. 1, no. 1
p. 100506
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No abstracts available.
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