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Results 1 - 10 of 16 for Nonsyndromic Deafness
  1. CDH23 gene 
    ... of 107 diverse families with Usher syndrome and nonsyndromic deafness. Am J Hum Genet. 2002 Aug;71(2): ... Friedman TB, Morell RJ. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  2. BSND gene 
    ... basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome. Am J Hum Genet. 2009 ...
    https://medlineplus.gov/genetics/gene/bsnd - Genetics
  3. TBC1D24 gene 
    ... TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. Am J Hum Genet. 2014 Jan 2;94(1):144-52. doi: 10.1016/j.ajhg.2013.12.004. Citation on PubMed or Free ... probable cause for nonsyndromic hearing impairment. Hum Mutat. 2014 Jul;35(7): ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  4. MYO7A gene 
    ... spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function. Hum Mutat. 2008 ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  5. WFS1 gene 
    ... other parts of the body. Individuals with DFNA6 nonsyndromic deafness cannot hear low tones (low-frequency sounds), such ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  6. MT-TS1 gene 
    ... 27. Citation on PubMed Usami SI, Nishio SY. Nonsyndromic Hearing Loss and Deafness, Mitochondrial. 2004 Oct 22 [updated 2018 Jun 14]. ...
    https://medlineplus.gov/genetics/gene/mt-ts1 - Genetics
  7. GJB2 gene 
    ... NBK1272/ Citation on PubMed Smith RJH, Ranum PT. Nonsyndromic Hearing Loss and Deafness, DFNA3 - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. 1998 ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  8. GJB6 gene 
    ... 0b013e32830e20b0. Citation on PubMed Smith RJH, Ranum PT. Nonsyndromic Hearing Loss and Deafness, DFNA3 - RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. 1998 ...
    https://medlineplus.gov/genetics/gene/gjb6 - Genetics
  9. POU3F4 gene 
    ... designated as DFNX2, sometimes also known as Nance deafness. DFNX2 is the most common type of X-linked nonsyndromic hearing loss, accounting for about half of all ...
    https://medlineplus.gov/genetics/gene/pou3f4 - Genetics
  10. ACTG1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about ... protein cytoskeletal gamma-actin deafness, autosomal dominant 20 deafness, autosomal dominant 26 DFNA20 ...
    https://medlineplus.gov/genetics/gene/actg1 - Genetics
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