[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene.

Cossu, G

[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

Publication Type: Journal Article

1526-632X

10.1212/01.WNL.0000148577.62644.77 doi


Adult
Female
Homozygote
Humans
Iodine Radioisotopes
Male
Mutation--genetics
Pantothenate Kinase-Associated Neurodegeneration--diagnosis
Phosphotransferases (Alcohol Group Acceptor)--genetics
Siblings
Tomography, Emission-Computed, Single-Photon--methods