SLC4A11 mutations in Fuchs endothelial corneal dystrophy. [electronic resource]
Producer: 20080314Description: 656-66 p. digitalISSN:- 1460-2083
- Adult
- Aged
- Aged, 80 and over
- Amino Acid Sequence
- Amino Acid Substitution
- Anion Transport Proteins -- genetics
- Antiporters -- genetics
- Asian People -- genetics
- Case-Control Studies
- Cohort Studies
- Conserved Sequence
- Female
- Frameshift Mutation
- Fuchs' Endothelial Dystrophy -- diagnosis
- Gene Deletion
- Genetic Testing
- Heterozygote
- Humans
- Male
- Middle Aged
- Models, Molecular
- Molecular Sequence Data
- Mutation, Missense
- Sequence Homology, Amino Acid
- Statistics as Topic
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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