Procaccio, V <br/><br/>
Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.  [electronic resource] 

 -  The Journal of clinical investigation  Jul 1999 
 - 83-92 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-9738 
<br/><br/><label>Standard No.: </label>10.1172/JCI6184  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acidosis, Lactic--congenital<br/>Cell Nucleus--chemistry<br/>Cells, Cultured<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>DNA, Complementary--genetics<br/>DNA, Mitochondrial--genetics<br/>Electron Transport<br/>Fatal Outcome<br/>Fibroblasts--enzymology<br/>Genetic Complementation Test<br/>Genetic Heterogeneity<br/>Humans<br/>Hybrid Cells<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Microscopy, Electron<br/>NAD(P)H Dehydrogenase (Quinone)--deficiency<br/>Organ Specificity<br/>Transcription, Genetic