Pepin, B <br/><br/>
Familial mitochondrial myopathy with cataract.  [electronic resource] 

 -  Journal of the neurological sciences  Mar 1980 
 - 191-203 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0022-510X 
<br/><br/><label>Standard No.: </label>10.1016/0022-510x(80)90165-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Cataract--genetics<br/>Child<br/>Female<br/>HLA Antigens--analysis<br/>Humans<br/>Male<br/>Microscopy, Electron<br/>Middle Aged<br/>Mitochondria, Muscle<br/>Muscles--pathology<br/>Muscular Diseases--genetics<br/>Ophthalmoplegia--genetics<br/>Pedigree<br/>Syndrome