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
Abstract excerpt
No abstract is available from the source.
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 0151d537-f19c-5c7f-96f9-2a74f9dfacf8
- DOI
- 10.1038/ejhg.2009.78
- PMCID
- PMC2986633
