Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family. [electronic resource]
Producer: 20131230Description: e63026 p. digitalISSN:- 1932-6203
- Adolescent
- Amino Acid Sequence
- Animals
- Asian People -- genetics
- Base Sequence
- DNA Mutational Analysis
- Exome -- genetics
- Female
- Hearing Loss, Sensorineural -- genetics
- Heterozygote
- Humans
- Male
- Membrane Proteins -- chemistry
- Mice
- Molecular Sequence Data
- Pedigree
- Polymorphism, Genetic
- Rats
- Siblings
- Young Adult
No physical items for this record
Publication Type: 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.