Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

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Detalhes bibliográficos
Main 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
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2009
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Corrigendum
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2986633/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2009.78
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