论文信息 - GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico. - 字舞流文

GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico.

L. E. Martínez-de-Villarreal | Á. Lugo‐Trampe | L. D. Campos-Acevedo | J. L. Treviño-Gonzalez | Aideé Alejandra Hernández-Juárez | J. Lugo-Trampe | Israel de-la-Cruz-Ávila | L. Martínez-de-Villarreal