Kodama, H <br/><br/>
Ornithine transcarbamylase deficiency: a case with a truncated enzyme precursor and a case with undetectable mRNA activity.  [electronic resource] 

 -  Journal of inherited metabolic disease  1986 
 - 175-85 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0141-8955 
<br/><br/><label>Standard No.: </label>10.1007/BF01799456  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Enzyme Precursors--biosynthesis<br/>Female<br/>Humans<br/>Immunologic Techniques<br/>Liver--enzymology<br/>Mitochondria, Liver--metabolism<br/>Molecular Weight<br/>Ornithine Carbamoyltransferase--genetics<br/>Ornithine Carbamoyltransferase Deficiency Disease<br/>Protein Biosynthesis<br/>Protein Processing, Post-Translational<br/>RNA, Messenger--metabolism