Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

✍ Scribed by Julie M. Bork; Linda M. Peters; Saima Riazuddin; Steve L. Bernstein; Zubair M. Ahmed; Seth L. Ness; Robert Polomeno; Arabandi Ramesh; Melvin Schloss; C. R. Srikumari Srisailpathy; Sigrid Wayne; Susan Bellman; Dilip Desmukh; Zahoor Ahmed; Shaheen N. Khan; Vazken M. Der Kaloustian; X. Cindy Li; Anil Lalwani; Sheikh Riazuddin; Maria Bitner-Glindzicz; Walter E. Nance; Xue-Zhong Liu; Graeme Wistow; Richard J.H. Smith; Andrew J. Griffith; Edward R. Wilcox; Thomas B. Friedman; Robert J. Morell

• Book ID: 117853509
• Publisher: American Society of Human Genetics
• Year: 2001
• Tongue: English
• Weight: 609 KB
• Volume: 68
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/316954