Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

Authors:	Bork J M Peters L M Riazuddin S Bernstein S L Ahmed Z M Ness S L Polomeno R Ramesh A Schloss M Srisailpathy C R Wayne S Bellman S Desmukh D Ahmed Z Khan S N Kaloustian V M Li X C Lalwani A Riazuddin S Bitner-Glindzicz M Nance W E Liu X Z Wistow G Smith R J Griffith A J Wilcox E R Friedman T B Morell R J

Affiliation:	Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.

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