A Novel Type of Myosin Encoded by the Mouse Deafness Geneshaker-2
- 1 July 1998
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 248 (3) , 655-659
- https://doi.org/10.1006/bbrc.1998.8976
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA geneNature Genetics, 1997
- Mutations in the myosin VIIA gene cause non-syndromic recessive deafnessNature Genetics, 1997
- Genetic and Physical Delineation of the Region of the Mouse Deafness Mutationshaker-2Biochemical and Biophysical Research Communications, 1997
- Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessNature, 1997
- Genes responsible for human hereditary deafness: symphony of a thousandNature Genetics, 1996
- Genetics of deafnessCurrent Opinion in Neurobiology, 1996
- Preferential isolation of DNA fragments associated with CpG islands.Proceedings of the National Academy of Sciences, 1995
- A type VII myosin encoded by the mouse deafness gene shaker-1Nature, 1995
- A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17Nature Genetics, 1995
- Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach.Proceedings of the National Academy of Sciences, 1991