A Novel SNCA A30G Mutation Causes Familial Parkinson's Disease

Liu, H; Koros, C; Strohaker, T; Schulte, C; Bozi, M; Varvaresos, S; de Opakua, AI; Simitsi, AM; Bougea, A; Voumvourakis, K; Maniati, M; Papageorgiou, SG; Hauser, AK; Becker, S; Zweckstetter, M; Stefanis, L; Gasser, T

Gasser, T (corresponding author), Univ Tubingen, Hertie Inst Clin Brain Res, Dept Neurodegenerat Dis, Tubingen, Germany.; Gasser, T (corresponding author), German Ctr Neurodegenerat Dis DZNE, Tubingen, Germany.; Stefanis, L (corresponding author), Natl & Kapodistrian Univ Athens, Attikon Hosp, Dept Neurol 2, Athens, Greece.; Zweckstetter, M (corresponding author), German Ctr Neurodegenerat Dis DZNE, Gottingen, Germany.

MOVEMENT DISORDERS, 2021; 36 (7): 1624

Abstract

Background The SNCA gene encoding alpha-synuclein (alpha Syn) is the first gene identified to cause autosomal-dominant Parkinson's disease (PD). Objec......

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