Pande, Suchita <br/><br/>
Biochemical and structural insights into an allelic variant causing the lysosomal storage disorder - aspartylglucosaminuria.  [electronic resource] 

 -  FEBS letters  08 2018 
 - 2550-2561 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1873-3468 
<br/><br/><label>Standard No.: </label>10.1002/1873-3468.13190  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Sequence<br/>Amino Acid Substitution--genetics<br/>Aspartylglucosaminuria--enzymology<br/>Aspartylglucosylaminase--chemistry<br/>Crystallography, X-Ray<br/>Finland<br/>Homeostasis--genetics<br/>Humans<br/>Lysosomal Storage Diseases--genetics<br/>Models, Molecular<br/>Point Mutation<br/>Protein Structure, Secondary<br/>Proteolysis