Morgan-Hughes, J A <br/><br/>
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.  [electronic resource] 

 -  Biochimica et biophysica acta  May 1995 
 - 135-40 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-3002 
<br/><br/><label>Standard No.: </label>10.1016/0925-4439(95)00020-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Biopsy<br/>Child<br/>Cytochrome b Group--genetics<br/>DNA, Mitochondrial--genetics<br/>Electron Transport Complex III--genetics<br/>Electron Transport Complex IV--genetics<br/>Female<br/>Genotype<br/>Humans<br/>MELAS Syndrome--genetics<br/>Male<br/>Middle Aged<br/>Mitochondrial Encephalomyopathies--genetics<br/>Muscle, Skeletal--metabolism<br/>NAD(P)H Dehydrogenase (Quinone)--genetics<br/>Phenotype<br/>Point Mutation<br/>RNA, Transfer, Leu--genetics