Bandmann, O <br/><br/>
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration.  [electronic resource] 

 -  Neurology  Dec 1997 
 - 1598-604 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.49.6.1598  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Animals<br/>Ciliary Neurotrophic Factor<br/>Genotype<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Insulin-Like Growth Factor I--metabolism<br/>Mice<br/>Mice, Neurologic Mutants--genetics<br/>Multiple System Atrophy--genetics<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Receptors, Somatomedin--genetics<br/>Repetitive Sequences, Nucleic Acid<br/>Sequence Homology, Nucleic Acid<br/>Spinocerebellar Degenerations--genetics