Correction to: European Journal of Human Genetics (2009) 17, 554–564; doi:10.1038/ejhg.2008.231; published online 24 December 2008
Since the publication of the above paper, the authors have identified the following errors in the paper:
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1)
Co-author XC Li should be replaced with Xiaoyan Cindy Li.
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2)
Co-author Larry Shotland should be replaced with Lawrence I Shotland, and his affiliation changed to the Hearing Section, NIDCD, NIH, Bethesda, Maryland, USA.
They also wish to state that ‘institutional review board approval (OH95-DC-N-050) was obtained from the National Institutes of Health, USA’. The project was also funded by Genome Canada (AMGGI).
The authors would like to apologise for the above mistakes.
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The online version of the original article can be found at 10.1038/ejhg.2008.231
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Doucette, L., Merner, N., Cooke, S. et al. Erratum: Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15. Eur J Hum Genet 17, 1363 (2009). https://doi.org/10.1038/ejhg.2009.78
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DOI: https://doi.org/10.1038/ejhg.2009.78
