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Published in 2018 at "Movement Disorders"
DOI: 10.1002/mds.27451
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).
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Keywords:
spect 123;
disease;
123i cit;
cit spect ... See more keywords