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α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism

Sokratous, M; Breza, M; Senkevich, K; Gan-Or, Z; Kalampokini, S; Spanaki, C; Provatas, A; ... Xiromerisiou, G; + view all (2021) α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism. Movement Disorders , 36 (9) pp. 2209-2212. 10.1002/mds.28735.

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Type: Article
Title: α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism
DOI: 10.1002/mds.28735
Publisher version: https://doi.org/10.1002/mds.28735
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, TRANSGENIC MICE
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/10139152
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