Matthes, Thomas <br/><br/>
Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion.  [electronic resource] 

 -  European journal of haematology  Aug 2006 
 - 169-74 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0902-4441 
<br/><br/><label>Standard No.: </label>10.1111/j.1600-0609.2006.00674.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acidosis--genetics<br/>Adolescent<br/>Anemia, Refractory--genetics<br/>Anemia, Sideroblastic--genetics<br/>Bone Marrow--pathology<br/>Cytochrome-c Oxidase Deficiency--genetics<br/>DNA Mutational Analysis<br/>DNA, Mitochondrial--genetics<br/>Disease Progression<br/>Electron Transport<br/>Electron Transport Complex IV--analysis<br/>Fatal Outcome<br/>Gene Deletion<br/>Heterozygote<br/>Humans<br/>Iron--metabolism<br/>Male<br/>Mitochondria--metabolism<br/>Mitochondrial Myopathies--blood<br/>Mitochondrial Proton-Translocating ATPases--deficiency<br/>Mosaicism<br/>RNA, Transfer--genetics<br/>beta-Thalassemia--genetics