Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families

✍ Scribed by Löppönen, Tuija; Dietz, Aarno; Väisänen, Marja-Leena; Valtonen, Hannu; Kosunen, Ari; Hyvärinen, Antti; Ignatius, Jaakko; Löppönen, Heikki

• Book ID: 111874581
• Publisher: Informa plc
• Year: 2012
• Tongue: English
• Weight: 781 KB
• Category: Article
• ISSN: 0001-6489
• DOI: 10.3109/00016489.2012.669498