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A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss

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  1. Article

    Open Access

    Dispersed DNA variants underlie hearing loss in South Florida’s minority population

    We analyzed the genetic causes of sensorineural hearing loss in racial and ethnic minorities of South Florida by reviewing demographic, phenotypic, and genetic data on 136 patients presenting to the Hereditary...

    LéShon Peart, Joanna Gonzalez, Dayna Morel Swols, Duygu Duman… in Human Genomics (2023)

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  2. Article

    Open Access

    Novel GPR156 variants confirm its role in moderate sensorineural hearing loss

    Hereditary hearing loss (HL) is a genetically heterogeneous disorder affecting people worldwide. The implementation of advanced sequencing technologies has significantly contributed to the identification of no...

    Memoona Ramzan, Nazim Bozan, Serhat Seyhan, Mohammad Faraz Zafeer… in Scientific Reports (2023)

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