Westermann, C M <br/><br/>
Decreased oxidative phosphorylation and PGAM deficiency in horses suffering from atypical myopathy associated with acquired MADD.  [electronic resource] 

 -  Molecular genetics and metabolism  Nov 2011 
 - 273-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1096-7206 
<br/><br/><label>Standard No.: </label>10.1016/j.ymgme.2011.07.022  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Aspartate Aminotransferases--blood<br/>Base Sequence<br/>Creatine--urine<br/>Creatine Kinase--blood<br/>DNA Primers--genetics<br/>Female<br/>Horse Diseases--metabolism<br/>Horses<br/>L-Lactate Dehydrogenase--blood<br/>Malonates--urine<br/>Mitochondrial Proton-Translocating ATPases--metabolism<br/>Molecular Sequence Data<br/>Multiple Acyl Coenzyme A Dehydrogenase Deficiency--blood<br/>Oxidative Phosphorylation<br/>Phosphoglycerate Mutase--deficiency<br/>Physical Conditioning, Animal<br/>Rhabdomyolysis--etiology<br/>Sequence Analysis, DNA<br/>Succinates--urine<br/>Uric Acid--urine