Parkinsonism due to A53E α‐synuclein gene mutation: Clinical, genetic, epigenetic, and biochemical features
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DOI: 10.1002/mds.27506
Abstract: SNCA mutations cause autosomal dominant parkinsonism and inform our understanding of the molecular underpinnings of synucleinopathies. The most recently identified mutation, p.Ala53Glu (A53E), has only been observed in Finland. The objectives of this study were… read more here.
Keywords: clinical genetic; epigenetic biochemical; biochemical features; genetic epigenetic ... See more keywords