Seranski, P <br/><br/>
RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients.  [electronic resource] 

 -  Gene  May 2001 
 - 69-76 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0378-1119 
<br/><br/><label>Standard No.: </label>10.1016/s0378-1119(01)00415-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Amino Acid Sequence<br/>Blotting, Northern<br/>Cell Line<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 17--genetics<br/>DNA--chemistry<br/>DNA, Complementary--chemistry<br/>Female<br/>Gene Deletion<br/>Gene Expression<br/>Humans<br/>Intellectual Disability--pathology<br/>Molecular Sequence Data<br/>Peptides--genetics<br/>Proteins--genetics<br/>Psychomotor Disorders--pathology<br/>RNA--genetics<br/>Sequence Analysis, DNA<br/>Sequence Homology, Amino Acid<br/>Syndrome<br/>Tissue Distribution<br/>Trans-Activators<br/>Transcription Factors<br/>Trinucleotide Repeats--genetics