Marín-García, José <br/><br/>
Cardiomyopathy associated with neurologic disorders and mitochondrial phenotype.  [electronic resource] 

 -  Journal of child neurology  Oct 2002 
 - 759-65 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0883-0738 
<br/><br/><label>Standard No.: </label>10.1177/08830738020170101701  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Cardiomyopathies--genetics<br/>Child<br/>Child, Preschool<br/>DNA, Mitochondrial<br/>Dystonia--pathology<br/>Electron Transport Complex I<br/>Female<br/>Friedreich Ataxia--pathology<br/>Gene Deletion<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Kearns-Sayre Syndrome--pathology<br/>Leigh Disease--pathology<br/>Male<br/>Mitochondria--genetics<br/>Mitochondrial Myopathies--genetics<br/>Muscle, Skeletal--pathology<br/>Mutation<br/>Myocardium--pathology<br/>NADH, NADPH Oxidoreductases--metabolism<br/>Neuromuscular Diseases--pathology<br/>Ophthalmoplegia--pathology<br/>Phenotype<br/>Seizures--pathology