ABMGG Clinical Genetics & Genomics
ABMGG Clinical Genetics and Genomics
Hearing Loss DisordersEnglish
Exam overviewPractice session
A newborn with bilateral hearing loss is evaluated. GJB2 sequencing identifies two pathogenic variants (compound heterozygous). What percentage of hereditary non-syndromic hearing loss is attributed to GJB2 (connexin 26)?
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