A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss.

✍ Scribed by Pera, Alejandra; Villamar, Manuela; Viñuela, Antonio; Gandía, Marta; Medà, Carme; Moreno, Felipe; Hernández-Chico, Concepción

• Book ID: 109848881
• Publisher: Nature Publishing Group
• Year: 2008
• Tongue: English
• Weight: 217 KB
• Volume: 16
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/ejhg.2008.30