Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89. [electronic resource]
Producer: 20130916Description: 132-40 p. digitalISSN:- 1537-6605
- Animals
- Case-Control Studies
- Chickens
- Cochlea -- metabolism
- Computational Biology -- methods
- Consanguinity
- Female
- Genetic Linkage
- Hair Cells, Auditory, Inner -- metabolism
- Haplotypes
- Hearing Loss -- enzymology
- Homozygote
- Humans
- Lysine-tRNA Ligase -- genetics
- Male
- Mice
- Mutation, Missense
- Pedigree
- Transfer RNA Aminoacylation
- Zebrafish -- embryology
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.