Ush1c216A knock-in mouse survives Katrina
- 1 March 2007
- journal article
- Published by Elsevier in Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
- Vol. 616 (1-2) , 139-144
Abstract
No abstract availableKeywords
Funding Information
- Louisiana Board of Regents
- Foundation Fighting Blindness
- National Science Foundation (EPS-0346411)
This publication has 5 references indexed in Scilit:
- The USH1C 216G?A splice-site mutation results in a 35-base-pair deletionHuman Genetics, 2004
- A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1CNature Genetics, 2000
- A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C geneNature Genetics, 2000
- Improved Splice Site Detection in GenieJournal of Computational Biology, 1997
- Localization of two genes for usher syndrome type I to chromosome 11Genomics, 1992