Copy number variants are a common cause of non-syndromic hearing loss
Genome Medicine2014Vol. 6(5), pp. 37–37
Citations Over TimeTop 10% of 2014 papers
Andrew Shearer, Diana L. Kolbe, Héla Azaiez, Christina M. Sloan, Kathy L. Frees, Amy E. Weaver, Erika T Clark, Carla Nishimura, E. Ann Black-Ziegelbein, Richard J. Smith
Abstract
CNVs are an important cause of NSHL and their detection must be included in comprehensive genetic testing for hearing loss.
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