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Results 1 - 10 of 98 for Hearing impairment
  1. WFS1 gene 
    ... of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease. Hum Mutat. 2003 ... Tranebjaerg L. Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  2. TECTA gene 
    ... mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus. Am J Med Genet ... A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations. Cell Physiol Biochem. 2004; ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  3. STRC gene 
    ... as a major contributor to pediatric bilateral sensorineural hearing impairment. Am J Med Genet A. 2012 Feb;158A( ... T. DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics. ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  4. COL11A2 gene 
    ... PL, Smith RJ, Cremers CW. Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13). ...
    https://medlineplus.gov/genetics/gene/col11a2 - Genetics
  5. MYO7A gene 
    ... D, Najmabadi H, Bahlo M, Smith RJ. Variable hearing impairment in a DFNB2 family with a novel MYO7A ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  6. MT-TS1 gene 
    ... Ablonczy M, Nemeth K, Fekete G. Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T> ... Citation on PubMed Usami SI, Nishio SY. Nonsyndromic Hearing Loss and Deafness, Mitochondrial. 2004 Oct 22 [updated 2018 ...
    https://medlineplus.gov/genetics/gene/mt-ts1 - Genetics
  7. SLC26A4 gene 
    ... F. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations. Eur ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics
  8. GJB3 gene 
    ... junction protein beta-3 associated with autosomal dominant hearing impairment. Nat Genet. 1998 Dec;20(4):370-3. ...
    https://medlineplus.gov/genetics/gene/gjb3 - Genetics
  9. TBC1D24 gene 
    ... gene TBC1D24 is a probable cause for nonsyndromic hearing impairment. Hum Mutat. 2014 Jul;35(7):814-8. ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  10. USH2A gene 
    ... missing or altered usherin protein leads to the hearing impairment and vision loss that are characteristic of Usher ... IIA, while other mutations cause retinitis pigmentosa without hearing loss. More About This Health Condition US2 USH2 USH2A_ ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics
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