Schuelke, Markus <br/><br/>
New nuclear encoded mitochondrial mutation illustrates pitfalls in prenatal diagnosis by biochemical methods.  [electronic resource] 

 -  Clinical chemistry  May 2002 
 - 772-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-9147 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acidosis, Lactic--congenital<br/>Electron Transport Complex I<br/>Female<br/>Humans<br/>Male<br/>Mitochondria--genetics<br/>NADH Dehydrogenase<br/>NADH, NADPH Oxidoreductases--deficiency<br/>Pedigree<br/>Pregnancy<br/>Prenatal Diagnosis--methods<br/>Proteins--genetics