Novel mutation in forkhead box G1 (FOXG1) gene in an Indian patient with Rett syndrome. [electronic resource]
Producer: 20140411Description: 109-12 p. digitalISSN:- 1879-0038
- Amino Acid Sequence
- Animals
- Child
- Female
- Forkhead Transcription Factors -- chemistry
- Frameshift Mutation
- Humans
- India
- Methyl-CpG-Binding Protein 2 -- genetics
- Molecular Sequence Data
- Nerve Tissue Proteins -- chemistry
- Protein Serine-Threonine Kinases -- genetics
- Rett Syndrome -- diagnosis
- Sequence Homology, Amino Acid
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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