The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis. [electronic resource]
Producer: 20060210Description: 2619-27 p. digitalISSN:- 0964-6906
- Amino Acid Sequence
- DNA Primers
- Electrophoretic Mobility Shift Assay
- Eyelashes -- abnormalities
- Fluorescent Antibody Technique
- Forkhead Transcription Factors -- genetics
- Humans
- Luciferases
- Lymphedema -- complications
- Models, Genetic
- Models, Molecular
- Molecular Sequence Data
- Mutagenesis, Site-Directed
- Mutation, Missense -- genetics
- Sequence Analysis, DNA
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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