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Paper Details

Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults.
Hum Genet
6
2021
EYA4, EYA4 gene, EYA4 gene variants, EYA4 variants, HL, Mobitz Type II AV block, cardiac conduction disorders, cardiac tissue, cardiomyopathy, children, hearing loss, human, participants, pleiotropic gene variants, syndromic hearing loss, wildtype controls
Author NameAffiliation
Binglan LiPerelman School of Medicine, University of Pennsylvania
Batsal DevkotaChildren's Hospital of Philadelphia
Batsal DevkotaChildren's Hospital of Philadelphia
Marijana VujkovicPerelman School of Medicine, University of Pennsylvania
Marijana VujkovicCorporal Michael J. Crescenz VA Medical Center
Ian D KrantzChildren's Hospital of Philadelphia
Marylyn D RitchiePerelman School of Medicine, University of Pennsylvania
Marylyn D RitchiePerelman School of Medicine, University of Pennsylvania
Daniel J RaderPerelman School of Medicine, University of Pennsylvania
Daniel J RaderPerelman School of Medicine at the University of Pennsylvania, 11-125 Smilow Center for Translational Research
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