Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes

✍ Scribed by Schultz, J. M.; Bhatti, R.; Madeo, A. C.; Turriff, A.; Muskett, J. A.; Zalewski, C. K.; King, K. A.; Ahmed, Z. M.; Riazuddin, S.; Ahmad, N.; Hussain, Z.; Qasim, M.; Kahn, S. N.; Meltzer, M. R.; Liu, X. Z.; Munisamy, M.; Ghosh, M.; Rehm, H. L.; Tsilou, E. T.; Griffith, A. J.; Zein, W. M.; Brewer, C. C.; Riazuddin, S.; Friedman, T. B.

• Book ID: 121868684
• Publisher: BMJ Publishing Group
• Year: 2011
• Tongue: English
• Weight: 486 KB
• Volume: 48
• Category: Article
• ISSN: 0022-2593
• DOI: 10.1136/jmedgenet-2011-100262