mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)
- 15 September 1997
- journal article
- Published by Elsevier BV in Genomics
- Vol. 44 (3), 266-272
- https://doi.org/10.1006/geno.1997.4869
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22Human Molecular Genetics, 1996
- A candidate gene for the mouse mutation tubbyNature, 1996
- The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteinsNature Genetics, 1996
- The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cellsNature Genetics, 1995
- A type VII myosin encoded by the mouse deafness gene shaker-1Nature, 1995
- A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalHuman Molecular Genetics, 1994
- A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 geneHuman Molecular Genetics, 1994
- Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strainsHearing Research, 1993
- Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouseGenetics Research, 1966
- The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouseProceedings of the Royal Society of London. Series B - Biological Sciences, 1956