Sharifi, Reza <br/><br/>
Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease.  [electronic resource] 

 -  The EMBO journal  May 2013 
 - 1225-37 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2075 
<br/><br/><label>Standard No.: </label>10.1038/emboj.2013.51  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Cells, Cultured<br/>Child<br/>Child, Preschool<br/>Family<br/>Female<br/>Glycoside Hydrolases--genetics<br/>HEK293 Cells<br/>HeLa Cells<br/>Humans<br/>Male<br/>Models, Molecular<br/>Molecular Sequence Data<br/>Neurodegenerative Diseases--enzymology<br/>Pedigree<br/>Poly Adenosine Diphosphate Ribose--genetics<br/>Protein Processing, Post-Translational--genetics<br/>Sequence Homology, Amino Acid<br/>Thiolester Hydrolases--genetics