A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

✍ Scribed by Del Castillo, F. J. (author);Rodríguez-Ballesteros, M. (author);Álvarez, A. (author);Hutchin, T. (author);Leonardi, E. (author);De Oliveira, C. A. (author);Azaiez, H. (author);Brownstein, Z. (author);Avenarius, M. R. (author);Marlin, S. (author);Pandya, A. (author);Shahin, H. (author);Siemering (author);Weil, D. (author);Wuyts, W. (author);Aguirre, L. A. (author);Marlín, Y. (author);Moreno-Pelayo, M. A. (author);Villamar, M. (author);Avraham, K. B. (author);Dahl, H. H.M. (author);Kanaan, M. (author);Nance, W. E. (author);Petit, C. (author);Smith, R. J.H. (author);Van Camp, G. (author);Sartorato, E. L. (author);Murgia, A. (author);Moreno, F. (author);Del Castillo, Ignacio (author)

• Book ID: 124096543
• Publisher: BMJ Publishing Group
• Year: 2005
• Tongue: English
• Weight: 139 KB
• Volume: 42
• Category: Article
• ISSN: 0022-2593
• DOI: 10.1136/jmg.2004.028324