Dadgar, Sharareh <br/><br/>
Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy.  [electronic resource] 

 -  Experimental eye research  Sep 2006 
 - 702-6 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0014-4835 
<br/><br/><label>Standard No.: </label>10.1016/j.exer.2006.03.004  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Animals<br/>GTP Phosphohydrolases--genetics<br/>Humans<br/>Models, Molecular<br/>Mutation, Missense<br/>Optic Atrophy, Autosomal Dominant--genetics<br/>Protein Structure, Tertiary<br/>Sequence Homology