Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42
- 1 February 2011
- journal article
- research article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 88 (2) , 127-137
Abstract
No abstract availableKeywords
Funding Information
- Deutsche Forschungsgemeinschaft (BO2985/3-1)
- National Institutes of Health (RO1 DC002842)
- International Centre for Genetic Engineering and Biotechnology
- National Institute on Deafness and Other Communication Disorders (DC000039-14)
- Higher Education Commission, Pakistan
- Johns Hopkins University (N01-HG-65403)
- Skaggs Institute for Chemical Biology, Scripps Research Institute
- National Health and Medical Research Council
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