Fragaki, Konstantina <br/><br/>
A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene.  [electronic resource] 

 -  Mitochondrion  Sep 2009 
 - 346-52 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1872-8278 
<br/><br/><label>Standard No.: </label>10.1016/j.mito.2009.06.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Cytochromes b--deficiency<br/>DNA, Mitochondrial--genetics<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Mitochondrial Diseases--genetics<br/>Multiple Organ Failure--genetics<br/>Mutation, Missense<br/>Point Mutation<br/>Young Adult