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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| Description | scientific article |
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author: Lance Doucette Terry-Lynn Young Nancy D Merner Mary-Claire King Tom Walsh |
| Publication date | December 24, 2008 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |