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- Title
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.
- Authors
Doucette, Lance; Merner, Nancy D; Cooke, Sandra; Ives, Elizabeth; Galutira, Dante; Walsh, Vanessa; Walsh, Tom; MacLaren, Linda; Cater, Tracey; Fernandez, Bridget; Green, Jane S; Wilcox, Edward R; Shotland, Larry; Li, X C; Lee, Ming; King, Mary-Claire; Young, Terry-Lynn
- Abstract
A correction to the article "Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15" that was published online in the December 24, 2008 issue is presented.
- Subjects
HUMAN genetics
- Publication
European Journal of Human Genetics, 2009, Vol 17, Issue 10, p1363
- ISSN
1018-4813
- Publication type
Correction notice
- DOI
10.1038/ejhg.2009.78