Bonifati, V <br/><br/>
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases.  [electronic resource] 

 -  Neuroscience letters  Oct 1999 
 - 61-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0304-3940 
<br/><br/><label>Standard No.: </label>10.1016/s0304-3940(99)00669-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Alleles<br/>DNA Mutational Analysis<br/>Exons--genetics<br/>Haplotypes<br/>Humans<br/>Introns--genetics<br/>Italy<br/>Mutation--genetics<br/>Protein Isoforms<br/>RNA Splicing--genetics<br/>Supranuclear Palsy, Progressive--genetics<br/>tau Proteins--genetics