Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

Authors:

Abstract
No abstract available
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

This publication has 37 references indexed in Scilit: