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Results 1 - 3 of 3 for "Deafness," autosomal recessive 26
  1. CDH23 gene 
    ... TB, Morell RJ. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet. 2001 Jan;68(1):26-37. doi: 10.1086/316954. Epub 2000 Nov ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  2. SLC26A4 gene 
    The SLC26A4 gene provides instructions for making a protein called pendrin. This protein transports negatively charged particles (ions), including chloride, ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics
  3. GJB2 gene 
    ... Verselis VK. Aberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: ... Autosomal Recessive Nonsyndromic Hearing Loss. 1998 Sep 28 [updated 2023 ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics