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The promoter mutation c.-259C>T (-3438C>T) is not a common cause of non-syndromic hearing impairment in Austria.
Koenighofer, Martin; Lucas, Trevor; Parzefall, Thomas; Ramsebner, Reinhard; Schoefer, Christian; Frei, Klemens.
Affiliation
  • Koenighofer M; Department of Otorhinolaryngology-Head and Neck Surgery, Medical University of Vienna, AKH 8J, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Eur Arch Otorhinolaryngol ; 272(1): 229-32, 2015 Jan.
Article in En | MEDLINE | ID: mdl-25085637
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Connexins / Hearing Loss / Mutation Type of study: Prevalence_studies / Risk_factors_studies Limits: Female / Humans / Male / Newborn Country/Region as subject: Europa Language: En Journal: Eur Arch Otorhinolaryngol Journal subject: OTORRINOLARINGOLOGIA Year: 2015 Document type: Article Affiliation country: Austria Country of publication: Germany
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / Connexins / Hearing Loss / Mutation Type of study: Prevalence_studies / Risk_factors_studies Limits: Female / Humans / Male / Newborn Country/Region as subject: Europa Language: En Journal: Eur Arch Otorhinolaryngol Journal subject: OTORRINOLARINGOLOGIA Year: 2015 Document type: Article Affiliation country: Austria Country of publication: Germany