Clark, L N <br/><br/>
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Oct 1998 
 - 13103-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.95.22.13103  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Aged<br/>Alternative Splicing<br/>Amino Acid Sequence<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 17<br/>Dementia--genetics<br/>Genetic Linkage<br/>Globus Pallidus--pathology<br/>Humans<br/>Introns<br/>Middle Aged<br/>Molecular Sequence Data<br/>Neurodegenerative Diseases--genetics<br/>Parkinson Disease--genetics<br/>Point Mutation<br/>Pons--pathology<br/>Repetitive Sequences, Amino Acid<br/>Sequence Alignment<br/>Sequence Homology, Amino Acid<br/>Substantia Nigra--pathology<br/>tau Proteins--chemistry