Mancuso, Michelangelo <br/><br/>
New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndrome.  [electronic resource] 

 -  Archives of neurology  May 2005 
 - 745-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.62.5.745  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blotting, Northern--methods<br/>DNA Mutational Analysis--methods<br/>Female<br/>Hepatic Encephalopathy--etiology<br/>Homozygote<br/>Humans<br/>Infant<br/>Liver--metabolism<br/>Mitochondrial Diseases--complications<br/>Muscles--metabolism<br/>Mutation<br/>Phosphotransferases (Alcohol Group Acceptor)--genetics<br/>RNA, Messenger--biosynthesis<br/>Reverse Transcriptase Polymerase Chain Reaction--methods<br/>Siblings