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

✍ Scribed by Merner, Nancy D; Cooke, Sandra; Ives, Elizabeth; Galutira, Dante; Walsh, Vanessa; Doucette, Lance; Walsh, Tom; MacLaren, Linda; Cater, Tracey; Fernandez, Bridget

• Book ID: 109849174
• Publisher: Nature Publishing Group
• Year: 2009
• Tongue: English
• Weight: 35 KB
• Volume: 17
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/ejhg.2009.78