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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

2009-09-24

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Literature Corpus work
0151d537-f19c-5c7f-96f9-2a74f9dfacf8
DOI
10.1038/ejhg.2009.78
PMCID
PMC2986633
Open publication

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Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15DOI 10.1038/ejhg.2009.78
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