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Results 1 - 6 of 6 for Autosomal dominant nonsyndromic hearing loss 12
  1. TECTA gene 
    ... in this gene can cause two forms of nonsyndromic hearing loss: DFNA8/12 and DFNB21.DFNA8/12 is inherited in an autosomal dominant pattern, which means one mutated copy of the ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  2. Nonsyndromic hearing loss 
    ... Casavant TL, Smith RJ, Moreno-Pelayo MA. DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss. Hum Mutat. 2011 Jul;32(7):825-34. ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  3. TBC1D24 gene 
    ... Black-Ziegelbein EA, Smith RJ. TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. Hum Mutat. 2014 Jul;35(7):819-23. ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  4. ACTG1 gene 
    ... in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26). J Med Genet. 2003 Dec;40(12):879-84. doi: 10.1136/jmg.40.12. ...
    https://medlineplus.gov/genetics/gene/actg1 - Genetics
  5. 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 ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  6. GJA1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Nonsyndromic hearing loss More About This Health Condition At least 76 ... K, Passos-Bueno MR, Reichenberger EJ. A novel autosomal recessive GJA1 ... dysplasia. PLoS One. 2013 Aug 12;8(8):e73576. doi: 10.1371/journal.pone. ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics