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Hyaluronan Synthase 1: A Novel Candidate Gene Associated With Late-Onset Non-syndromic Hereditary Hearing Loss
Alphonse Umugire, Sungsu Lee, Chang-Joon Lee, Youngmi Choi, Taekyoung Kim, Hyong-Ho Cho
Clinical and Experimental Otorhinolaryngology. 2022;15(3):220-229.   Published online 2022 April 8    DOI: https://doi.org/10.21053/ceo.2022.00038

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Hyaluronan Synthase 1: A Novel Candidate Gene Associated With Late-Onset Non-syndromic Hereditary Hearing Loss
Clinical and Experimental Otorhinolaryngology. 2022;15(3):220-229   Crossref logo
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Gene mapping of non-syndromic hereditary hearing loss
International Journal of Pediatric Otorhinolaryngology. 1997;39(3):246-247   Crossref logo
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Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses
Hearing Research. 2002;166(1-2):150-158   Crossref logo
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A novel splice site mutation in DFNA5 causes late-onset progressive non-syndromic hearing loss in a Chinese family
International Journal of Pediatric Otorhinolaryngology. 2014;78(8):1265-1268   Crossref logo
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Hereditary Non-Syndromic Sensorineural Hearing Loss
The Journal of Molecular Diagnostics. 2004;6(4):275-284   Crossref logo
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Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families
Clinical Genetics. 2007;72(3):261-263   Crossref logo
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A novel dominant missense mutation - D179N - in theGJB2gene (Connexin 26) associated with non-syndromic hearing loss
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A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
Gene. 2015;574(1):28-33   Crossref logo
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Variants in CDH23 Cause Broad Spectrum of Hearing Loss: From Non-Syndromic to Syndromic Hearing Loss as Well as From Congenital to Age-Related Hearing Loss
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Whole Exome Sequencing of Six Chinese Families with Hereditary Non-syndromic Hearing Loss
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