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The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.
Schütz, Melanie; Scimemi, Pietro; Majumder, Paromita; De Siati, Romolo Daniele; Crispino, Giulia; Rodriguez, Laura; Bortolozzi, Mario; Santarelli, Rosamaria; Seydel, Anke; Sonntag, Stephan; Ingham, Neil; Steel, Karen P; Willecke, Klaus; Mammano, Fabio.
Affiliation
  • Schütz M; Institut fuer Genetik, Rheinische Friedrich-Wilhelms-Universitaet Bonn, Roemerstrasse 164, D-53117 Bonn, Germany.
Hum Mol Genet ; 19(24): 4759-73, 2010 Dec 15.
Article in En | MEDLINE | ID: mdl-20858605
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cochlea / Connexins / Deafness / Hearing Loss, Bilateral / Mutation Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2010 Document type: Article Affiliation country: Germany Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cochlea / Connexins / Deafness / Hearing Loss, Bilateral / Mutation Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2010 Document type: Article Affiliation country: Germany Country of publication: United kingdom