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Nonsyndromic Hearing "Loss," Dominant
- ... TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss. Hum Mutat. 2011 Jul;32(7):825-34. ...
- ... genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation. ...
- ... Ziegelbein EA, Smith RJ. TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. Hum Mutat. 2014 Jul;35(7):819-23. ...
- ... in this gene can cause two forms of nonsyndromic hearing loss: DFNA13 and DFNB53.DFNA13 is inherited in an autosomal dominant pattern, which means only one mutated copy of ...
- ... gene are thought to cause two forms of nonsyndromic hearing loss: DFNA11 and DFNB2.DFNA11 is inherited in an autosomal dominant pattern, which means only one mutated copy of ...
- ... This Health Condition MedlinePlus Genetics provides information about ... gamma-actin deafness, autosomal dominant 20 deafness, autosomal dominant 26 DFNA20 DFNA26 gamma- ...
- ... Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing ... with nonsyndromic hearing loss. Biochim Biophys Acta. 2013 Jan;1832( ...
- ... than 100 GJB2 gene mutations that can cause nonsyndromic hearing loss, which is loss of hearing that is not ... in this gene can cause two forms of nonsyndromic hearing loss: DFNB1 and DFNA3.DFNB1 is inherited in an ...
- ... a few GJB6 gene mutations in individuals with nonsyndromic hearing loss, which is loss of hearing that is not ... Mutations in this gene cause a form of nonsyndromic hearing loss called DFNA3. This form of hearing loss can ...
- ... been identified in individuals with a form of nonsyndromic hearing loss called DFNA6. People with this condition have hearing ... R, Shelton C, Lalwani AK. Two families with nonsyndromic low-frequency hearing loss harbor novel mutations in Wolfram syndrome gene 1. ...