Concepedia

Publication | Open Access

Copy number variants are a common cause of non-syndromic hearing loss

DOIFull Paper Access

190

Citations

29

References

2014

Year

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
Genome Medicine

Abstract

CNVs are an important cause of NSHL and their detection must be included in comprehensive genetic testing for hearing loss.

References

YearCitations

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