Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family. [electronic resource]
Producer: 20090610Description: 241-50 p. digitalISSN:- 1673-8527
- Adult
- Asian People -- ethnology
- Base Sequence
- Connexin 26
- Connexins -- genetics
- Deafness -- ethnology
- Female
- Genetic Variation
- Humans
- Male
- Middle Aged
- Mitochondria -- chemistry
- Mitochondrial Proteins -- genetics
- Nucleic Acid Conformation
- Pedigree
- Phenotype
- Point Mutation
- RNA, Ribosomal -- chemistry
- RNA, Transfer, Gly -- chemistry
- tRNA Methyltransferases -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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