"123I‐FP‐CIT SPECT [(123) I‐2β‐carbomethoxy‐3β‐(4‐iodophenyl)‐N‐(3‐fluoropropyl) nortropane single photon emission computed tomography] Imaging in a p.A53T α‐synuclein Parkinson's disease cohort versus Parkinson's disease"

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123I‐FP‐CIT SPECT [(123) I‐2β‐carbomethoxy‐3β‐(4‐iodophenyl)‐N‐(3‐fluoropropyl) nortropane single photon emission computed tomography] Imaging in a p.A53T α‐synuclein Parkinson's disease cohort versus Parkinson's disease

Background: The p.A53T point mutation in the α‐synuclein gene (SNCA) is a rare but highly relevant cause of autosomal dominant Parkinson's disease (PD). Click to show full abstract

Background: The p.A53T point mutation in the α‐synuclein gene (SNCA) is a rare but highly relevant cause of autosomal dominant Parkinson's disease (PD).

Keywords: spect 123; disease; 123i cit; cit spect; parkinson disease

Journal Title: Movement Disorders
Year Published: 2018

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