Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

✍ Scribed by Ahmed, Zubair M; Masmoudi, Saber; Kalay, Ersan; Belyantseva, Inna A; Mosrati, Mohamed Ali; Collin, Rob W J; Riazuddin, Saima; Hmani-Aifa, Mounira; Venselaar, Hanka; Kawar, Mayya N

• Book ID: 109914334
• Publisher: Nature Publishing Group
• Year: 2008
• Tongue: English
• Weight: 725 KB
• Volume: 40
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng.245