Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23
Julie M. Bork(National Institutes of Health), Linda Peters(National Institutes of Health), Saima Riazuddin(National Institutes of Health), Steven L. Bernstein(University of Maryland, Baltimore), Zubair M. Ahmed(National Institutes of Health), Seth Ness(Mount Sinai Medical Center), Robert C. Polomeno(McGill University), Arabandi Ramesh(University of Iowa), Melvin D. Schloss(McGill University), C.R. Srikumari Srisailpathy(University of Iowa), Sigrid Wayne(University of Iowa), Susan Bellman(Great Ormond Street Hospital), Dilip Desmukh, Zahoor Ahmed(National Institutes of Health), Shaheen N. Khan(University of the Punjab), Vazken M. Der Kaloustian(McGill University), X. Cindy Li(National Institutes of Health), Anil K. Lalwani, Sheikh Riazuddin(University of the Punjab), Maria Bitner‐Glindzicz(Institute of Child Health), Walter E. Nance(Virginia Commonwealth University Medical Center), Xue Zhong Liu(Virginia Commonwealth University Medical Center), Graeme Wistow(National Institutes of Health), Richard J. Smith(University of Iowa), Andrew J. Griffith(National Institutes of Health), Edward R. Wilcox(National Institutes of Health), Thomas B. Friedman(National Institutes of Health), Robert J. Morell(National Institutes of Health)
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