Cossu, G <br/><br/>
[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene.  [electronic resource] 

 -  Neurology  Jan 2005 
 - 167-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.WNL.0000148577.62644.77  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Female<br/>Homozygote<br/>Humans<br/>Iodine Radioisotopes<br/>Male<br/>Mutation--genetics<br/>Pantothenate Kinase-Associated Neurodegeneration--diagnosis<br/>Phosphotransferases (Alcohol Group Acceptor)--genetics<br/>Siblings<br/>Tomography, Emission-Computed, Single-Photon--methods