Hellenbroich, Y <br/><br/>
Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration.  [electronic resource] 

 -  Journal of neural transmission (Vienna, Austria : 1996)  Jul 2006 
 - 829-43 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0300-9564 
<br/><br/><label>Standard No.: </label>10.1007/s00702-005-0362-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Auditory Diseases, Central--genetics<br/>Brain Stem--pathology<br/>Cerebellum--pathology<br/>DNA Mutational Analysis<br/>Deglutition Disorders--genetics<br/>Female<br/>Genotype<br/>Germany<br/>Humans<br/>Immunohistochemistry<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Nerve Degeneration--pathology<br/>Neurons--pathology<br/>Ocular Motility Disorders--genetics<br/>Pedigree<br/>Peptides--genetics<br/>Sensation Disorders--genetics<br/>Spinocerebellar Ataxias--genetics<br/>Trinucleotide Repeat Expansion--genetics