Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

詳細情報 詳細情報について

• CRID

  1360011145244965120

• DOI

  10.7150/thno.38032

• ISSN

  18387640

• Web Site

  http://www.thno.org/v09p7184.htm

• データソース種別

  • Crossref