Obara-Moszynska, Monika <br/><br/>
A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment.  [electronic resource] 

 -  BMC pediatrics  Feb 2013 
 - 27 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1471-2431 
<br/><br/><label>Standard No.: </label>10.1186/1471-2431-13-27  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Atrioventricular Block--diagnosis<br/>Base Sequence<br/>Cardiomyopathy, Dilated--diagnosis<br/>DNA, Mitochondrial<br/>Fatal Outcome<br/>Growth Disorders--drug therapy<br/>Human Growth Hormone--deficiency<br/>Humans<br/>Kearns-Sayre Syndrome--complications<br/>Male<br/>Recombinant Proteins<br/>Sequence Deletion