Kleyn, P W <br/><br/>
Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus.  [electronic resource] 

 -  Neurology  Sep 1991 
 - 1418-22 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.41.9.1418  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>DNA--analysis<br/>Electrophoresis<br/>G(M2) Activator Protein<br/>Gene Amplification<br/>Genes<br/>Hexosaminidase B<br/>Humans<br/>Molecular Sequence Data<br/>Muscular Atrophy, Spinal--enzymology<br/>Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Proteins--genetics<br/>beta-N-Acetylhexosaminidases--genetics