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Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss - Journal of Human Genetics

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Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss - Journal of Human Genetics

Hearing loss (HL) is a common heterogeneous trait that involves variants in more than 200 genes. In this study, we utilized exome (ES) and genome sequencing (GS) to effectively identify the genetic cause of presumably non-syndromic HL in 322 families from South and West Asia and Latin America. Biallelic GJB2 variants were identified in 58 probands at the time of enrollment these probands were excluded.

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Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss - Journal of Human Genetics

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Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss - Journal of Human Genetics

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