Lin, C Y <br/><br/>
Identification of a de Novo point mutation resulting in infantile form of Pompe's disease.  [electronic resource] 

 -  Biochemical and biophysical research communications  Aug 1995 
 - 367 p.  digital 
<br/><br/> Publication Type: Published Erratum 
<br/><br/><label>ISSN: </label>0006-291X 
<br/><br/><label>Standard No.: </label>10.1006/bbrc.1995.2139  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Aspartic Acid<br/>Base Sequence<br/>Codon<br/>Glycogen Storage Disease Type II--genetics<br/>Humans<br/>Infant<br/>Molecular Sequence Data<br/>Point Mutation<br/>alpha-Glucosidases--genetics