Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics. [electronic resource]
Producer: 20130107Description: 395-403 p. digitalISSN:- 1399-0004
- Adult
- Blotting, Western
- Child
- Chromatin -- metabolism
- Chromosomes, Human, Pair 15 -- genetics
- DNA Methylation -- genetics
- Female
- Fluorescence Recovery After Photobleaching
- Forkhead Transcription Factors -- genetics
- Genetic Diseases, Inborn -- genetics
- Humans
- Karyotyping
- Microscopy, Fluorescence
- Nerve Tissue Proteins -- genetics
- Phenotype
- Point Mutation -- genetics
- Syndrome
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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