Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss. [electronic resource]
Producer: 20030722Description: 1571-7 p. digitalISSN:- 0002-9297
- Amino Acid Substitution
- Animals
- Calmodulin-Binding Proteins
- Child
- Cochlea -- metabolism
- Codon, Nonsense -- genetics
- Female
- Hearing Loss, Sensorineural -- genetics
- Humans
- Male
- Mice
- Models, Molecular
- Molecular Sequence Data
- Mutagenesis, Insertional -- genetics
- Myosin Heavy Chains -- genetics
- Myosin Type I
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.