Genetic inactivation of Trpml3 does not lead to hearing and vestibular impairment in mice. [electronic resource]
Producer: 20110705Description: e14317 p. digitalISSN:- 1932-6203
- Animals
- Brain Stem -- physiology
- Cations
- Cell Line
- Cytosol -- metabolism
- Exons
- Gene Deletion
- Genotype
- Hearing -- genetics
- Hearing Loss -- genetics
- Humans
- Hydrogen -- chemistry
- Mice
- Mice, Knockout
- Models, Genetic
- Mutation
- Phenotype
- Protein Isoforms
- Sodium -- chemistry
- TRPM Cation Channels -- genetics
- Transient Receptor Potential Channels
- Vestibular Diseases -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural
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