Takehisa, Y <br/><br/>
Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions.  [electronic resource] 

 -  Archives of neurology  May 2001 
 - 736-40 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.58.5.736  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Amino Acid Substitution<br/>Amyotrophic Lateral Sclerosis--genetics<br/>Brain--pathology<br/>Female<br/>Humans<br/>Hyalin--ultrastructure<br/>Inclusion Bodies--ultrastructure<br/>Lewy Bodies--ultrastructure<br/>Male<br/>Middle Aged<br/>Point Mutation--genetics<br/>Superoxide Dismutase--genetics