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Results 1 - 6 of 6 for "Deafness," autosomal dominant 16
  1. DNMT1 gene 
    ... doi: 10.4161/epi.21568. Epub 2012 Aug 16. Citation on PubMed or Free article on ... cerebellar ataxia, deafness, and narcolepsy. Clin Epigenetics. 2016 Sep 5;8( ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  2. ACTG1 gene 
    ... gamma 1 actin-like protein cytoskeletal gamma-actin deafness, autosomal dominant 20 deafness, autosomal dominant 26 DFNA20 DFNA26 gamma-actin Tests of ACTG1 ...
    https://medlineplus.gov/genetics/gene/actg1 - Genetics
  3. WFS1 gene 
    ... Kunst HP, Hoefsloot EH, Cruysberg JR, Cremers CW. Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1. Mol Vis. 2010 Jan 12;16:26-35. Citation on PubMed or Free article ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  4. MYO7A gene 
    ... F, Drira M, Ayadi H, Petit C. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. Nat Genet. 1997 Jun;16(2):191-3. doi: 10.1038/ng0697-191. ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  5. GJB2 gene 
    ... Curr Opin Otolaryngol Head Neck Surg. 2008 Oct;16(5):452-7. doi: ... Autosomal Recessive Nonsyndromic Hearing Loss. 1998 Sep 28 [updated ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  6. TBC1D24 gene 
    ... Black-Ziegelbein EA, Smith RJ. TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. Hum Mutat. 2014 Jul;35( ... a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. Am J Hum ... T, Wu H. A dominant mutation in the stereocilia-expressing gene TBC1D24 is ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics