Delettre, Cécile <br/><br/>
OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease.  [electronic resource] 

 -  Molecular genetics and metabolism  Feb 2002 
 - 97-107 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1096-7192 
<br/><br/><label>Standard No.: </label>10.1006/mgme.2001.3278  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Chromosomes, Human, Pair 3<br/>GTP Phosphohydrolases--genetics<br/>Humans<br/>Mitochondrial Diseases--genetics<br/>Mutation<br/>Optic Atrophy, Autosomal Dominant--genetics<br/>Retinal Ganglion Cells--physiology<br/>Sequence Deletion