MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

✍ Scribed by Salvatore Melchionda; Nadav Ahituv; Luigi Bisceglia; Tama Sobe; Fabian Glaser; Raquel Rabionet; Maria Lourdes Arbones; Angelo Notarangelo; Enzo Di Iorio; Massimo Carella; Leopoldo Zelante; Xavier Estivill; Karen B. Avraham; Paolo Gasparini

• Book ID: 117853682
• Publisher: American Society of Human Genetics
• Year: 2001
• Tongue: English
• Weight: 844 KB
• Volume: 69
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/323156