Barth, Peter G <br/><br/>
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update.  [electronic resource] 

 -  American journal of medical genetics. Part A  May 2004 
 - 349-54 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.20660  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Acyltransferases<br/>Cardiolipins--analysis<br/>Cardiomyopathy, Dilated--pathology<br/>Female<br/>Genetic Diseases, X-Linked--genetics<br/>Humans<br/>Lipids--blood<br/>Male<br/>Muscular Diseases--pathology<br/>Mutation<br/>Neutropenia--pathology<br/>Pedigree<br/>Proteins--genetics<br/>Survival Rate<br/>Syndrome<br/>Transcription Factors--genetics