Allikmets, R <br/><br/>
Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A).  [electronic resource] 

 -  Human molecular genetics  May 1999 
 - 743-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/8.5.743  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATP-Binding Cassette Transporters--drug effects<br/>Amino Acid Sequence<br/>Amino Acid Substitution<br/>Anemia, Sideroblastic--genetics<br/>Blotting, Northern<br/>Cerebellar Ataxia--genetics<br/>Cloning, Molecular<br/>Female<br/>Ferrous Compounds--pharmacology<br/>Fungal Proteins--drug effects<br/>Genetic Complementation Test<br/>Humans<br/>Iron--metabolism<br/>Male<br/>Mitochondria--metabolism<br/>Molecular Sequence Data<br/>Mutation<br/>Saccharomyces cerevisiae--drug effects<br/>Saccharomyces cerevisiae Proteins<br/>X Chromosome