Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes

Overview of attention for article published in Frontiers in Genetics, August 2022

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New Research: Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes: Hearing loss (HL) is a common sensory deficit in humans and… https://t.co/bWS

30 Aug 2022

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