RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients. [electronic resource]
Producer: 20010802Description: 69-76 p. digitalISSN:- 0378-1119
- Abnormalities, Multiple -- genetics
- Amino Acid Sequence
- Blotting, Northern
- Cell Line
- Chromosome Deletion
- Chromosomes, Human, Pair 17 -- genetics
- DNA -- chemistry
- DNA, Complementary -- chemistry
- Female
- Gene Deletion
- Gene Expression
- Humans
- Intellectual Disability -- pathology
- Molecular Sequence Data
- Peptides -- genetics
- Proteins -- genetics
- Psychomotor Disorders -- pathology
- RNA -- genetics
- Sequence Analysis, DNA
- Sequence Homology, Amino Acid
- Syndrome
- Tissue Distribution
- Trans-Activators
- Transcription Factors
- Trinucleotide Repeats -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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