Ban, Yuriko <br/><br/>
A novel mutation of the OPA1 gene in a Japanese patient with autosomal dominant optic atrophy.  [electronic resource] 

 -  Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie  Oct 2007 
 - 1581-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>0721-832X 
<br/><br/><label>Standard No.: </label>10.1007/s00417-007-0598-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Asian People--genetics<br/>DNA Mutational Analysis<br/>Exons<br/>GTP Phosphohydrolases--genetics<br/>Humans<br/>Male<br/>Mutation<br/>Optic Atrophy, Autosomal Dominant--diagnosis<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Polymorphism, Single Nucleotide<br/>Sequence Analysis, DNA<br/>Tomography, Optical Coherence<br/>Visual Acuity<br/>Visual Fields