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Newborn Screening for Common Genetic Variants Associated with Permanent Hearing Loss: Implementation in Ontario and a Review of the First 3 Years

Kristin D. Kernohan, Lauren Gallagher, Marie Pigeon,Ed Yeh,Melanie Lacaria,Michelle M. Axford,Johnna MacCormick,Vicky Papaioannou,Nada Quercia, Charles Rupar, Kim Zimmerman, Stacey Weber,Sharon L. Cushing,Pranesh Chakraborty

Genetics in Medicine（2025）

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Key words
Permanent hearing loss,GJB2,SLC26A4,Newborn screening,Universal newborn hearing screening
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